Name: rs6662618
Published: September 21, 2022
License: Open Access

Welcome to the Reference SNP (rs) Report

All alleles are reported in the Forward orientation. Click on the Variant Details tab for details on Genomic Placement, Gene, and Amino Acid changes. HGVS names are in the HGVS tab.

Reference SNP (rs) Report

This page reports data for a single dbSNP Reference SNP variation (RefSNP or rs) from the new redesigned dbSNP build.
Top of the page reports a concise summary for the rs, with more specific details included in the corresponding tabs below.
All alleles are reported in the Forward orientation. Use the Genomic View to inspect the nucleotides flanking the variant, and its neighbors.
For more information see Help documentation.

rs6662618

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr1:92469854 (GRCh38.p14) Help
The anchor position for this RefSNP. Includes all nucleotides potentially affected by this change, thus it can differ from HGVS, which is right-shifted. See here for details.
Alleles: T>G
Variation Type: SNV Single Nucleotide Variation
Frequency: T=0.257127 (68059/264690, TOPMED)
T=0.173609 (35603/205076, GENOGRAPHIC)
T=0.182065 (37047/203482, ALFA) (+ 21 more)
T=0.249379 (34911/139992, GnomAD)
T=0.01469 (415/28256, 14KJPN)
T=0.01569 (263/16760, 8.3KJPN)
T=0.2442 (1564/6404, 1000G_30x)
T=0.2350 (1177/5008, 1000G)
T=0.1547 (693/4480, Estonian)
T=0.1741 (671/3854, ALSPAC)
T=0.1764 (654/3708, TWINSUK)
T=0.0160 (47/2930, KOREAN)
T=0.2202 (459/2084, HGDP_Stanford)
T=0.2587 (489/1890, HapMap)
T=0.0087 (16/1832, Korea1K)
T=0.1221 (138/1130, Daghestan)
T=0.152 (152/998, GoNL)
T=0.150 (90/600, NorthernSweden)
T=0.120 (62/516, SGDP_PRJ)
T=0.213 (46/216, Qatari)
T=0.046 (10/216, Vietnamese)
T=0.20 (11/54, Siberian)
T=0.17 (7/40, GENOME_DK)
T=0.20 (6/30, Ancient Sardinia)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: None
Publications: 2 citations
Genomic View: See rs on genome

ALFA Allele Frequency
The ALFA project provide aggregate allele frequency from dbGaP. More information is available on the project page including descriptions, data access, and terms of use.

Release Version: 20231103111315

Population	Group	Sample Size	Ref Allele	Alt Allele	Ref HMOZ	Alt HMOZ	HTRZ	HWEP
Total	Global	203482	T=0.182065	G=0.817935	0.037055	0.672924	0.290021	32
European	Sub	172556	T=0.169122	G=0.830878	0.029231	0.690987	0.279782	1
African	Sub	7764	T=0.4293	G=0.5707	0.185729	0.327151	0.48712	0
African Others	Sub	276	T=0.424	G=0.576	0.173913	0.326087	0.5	0
African American	Sub	7488	T=0.4295	G=0.5705	0.186165	0.32719	0.486645	0
Asian	Sub	750	T=0.035	G=0.965	0.0	0.930667	0.069333	0
East Asian	Sub	572	T=0.019	G=0.981	0.0	0.961538	0.038462	0
Other Asian	Sub	178	T=0.084	G=0.916	0.0	0.831461	0.168539	0
Latin American 1	Sub	990	T=0.291	G=0.709	0.09899	0.517172	0.383838	2
Latin American 2	Sub	9064	T=0.2253	G=0.7747	0.054722	0.604148	0.34113	2
South Asian	Sub	5054	T=0.1294	G=0.8706	0.019786	0.760981	0.219232	1
Other	Sub	7304	T=0.2082	G=0.7918	0.049288	0.632804	0.317908	3

Frequency tab displays a table of the reference and alternate allele frequencies reported by various studies and populations. Table lines, where Population="Global" refer to the entire study population, whereas lines, where Group="Sub", refer to a study-specific population subgroupings (i.e. AFR, CAU, etc.), if available. Frequency for the alternate allele (Alt Allele) is a ratio of samples observed-to-total, where the numerator (observed samples) is the number of chromosomes in the study with the minor allele present (found in "Sample size", where Group="Sub"), and the denominator (total samples) is the total number of all chromosomes in the study for the variant (found in "Sample size", where Group="Study-wide" and Population="Global").

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Study	Population	Group	Sample Size	Ref Allele	Alt Allele
TopMed	Global	Study-wide	264690	T=0.257127	G=0.742873
Genographic Project	Global	Study-wide	205076	T=0.173609	G=0.826391
Allele Frequency Aggregator	Total	Global	203482	T=0.182065	G=0.817935
Allele Frequency Aggregator	European	Sub	172556	T=0.169122	G=0.830878
Allele Frequency Aggregator	Latin American 2	Sub	9064	T=0.2253	G=0.7747
Allele Frequency Aggregator	African	Sub	7764	T=0.4293	G=0.5707
Allele Frequency Aggregator	Other	Sub	7304	T=0.2082	G=0.7918
Allele Frequency Aggregator	South Asian	Sub	5054	T=0.1294	G=0.8706
Allele Frequency Aggregator	Latin American 1	Sub	990	T=0.291	G=0.709
Allele Frequency Aggregator	Asian	Sub	750	T=0.035	G=0.965
gnomAD - Genomes	Global	Study-wide	139992	T=0.249379	G=0.750621
gnomAD - Genomes	European	Sub	75870	T=0.15790	G=0.84210
gnomAD - Genomes	African	Sub	41874	T=0.43005	G=0.56995
gnomAD - Genomes	American	Sub	13648	T=0.25418	G=0.74582
gnomAD - Genomes	Ashkenazi Jewish	Sub	3324	T=0.2479	G=0.7521
gnomAD - Genomes	East Asian	Sub	3124	T=0.0291	G=0.9709
gnomAD - Genomes	Other	Sub	2152	T=0.2505	G=0.7495
14KJPN	JAPANESE	Study-wide	28256	T=0.01469	G=0.98531
8.3KJPN	JAPANESE	Study-wide	16760	T=0.01569	G=0.98431
1000Genomes_30x	Global	Study-wide	6404	T=0.2442	G=0.7558
1000Genomes_30x	African	Sub	1786	T=0.4770	G=0.5230
1000Genomes_30x	Europe	Sub	1266	T=0.1848	G=0.8152
1000Genomes_30x	South Asian	Sub	1202	T=0.1572	G=0.8428
1000Genomes_30x	East Asian	Sub	1170	T=0.0205	G=0.9795
1000Genomes_30x	American	Sub	980	T=0.270	G=0.730
1000Genomes	Global	Study-wide	5008	T=0.2350	G=0.7650
1000Genomes	African	Sub	1322	T=0.4781	G=0.5219
1000Genomes	East Asian	Sub	1008	T=0.0198	G=0.9802
1000Genomes	Europe	Sub	1006	T=0.1849	G=0.8151
1000Genomes	South Asian	Sub	978	T=0.153	G=0.847
1000Genomes	American	Sub	694	T=0.272	G=0.728
Genetic variation in the Estonian population	Estonian	Study-wide	4480	T=0.1547	G=0.8453
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	T=0.1741	G=0.8259
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	T=0.1764	G=0.8236
KOREAN population from KRGDB	KOREAN	Study-wide	2930	T=0.0160	G=0.9840
HGDP-CEPH-db Supplement 1	Global	Study-wide	2084	T=0.2202	G=0.7798
HGDP-CEPH-db Supplement 1	Est_Asia	Sub	470	T=0.047	G=0.953
HGDP-CEPH-db Supplement 1	Central_South_Asia	Sub	414	T=0.164	G=0.836
HGDP-CEPH-db Supplement 1	Middle_Est	Sub	350	T=0.209	G=0.791
HGDP-CEPH-db Supplement 1	Europe	Sub	320	T=0.216	G=0.784
HGDP-CEPH-db Supplement 1	Africa	Sub	242	T=0.591	G=0.409
HGDP-CEPH-db Supplement 1	America	Sub	216	T=0.389	G=0.611
HGDP-CEPH-db Supplement 1	Oceania	Sub	72	T=0.00	G=1.00
HapMap	Global	Study-wide	1890	T=0.2587	G=0.7413
HapMap	American	Sub	770	T=0.153	G=0.847
HapMap	African	Sub	690	T=0.484	G=0.516
HapMap	Asian	Sub	254	T=0.008	G=0.992
HapMap	Europe	Sub	176	T=0.199	G=0.801
Korean Genome Project	KOREAN	Study-wide	1832	T=0.0087	G=0.9913
Genome-wide autozygosity in Daghestan	Global	Study-wide	1130	T=0.1221	G=0.8779
Genome-wide autozygosity in Daghestan	Daghestan	Sub	626	T=0.097	G=0.903
Genome-wide autozygosity in Daghestan	Near_East	Sub	142	T=0.204	G=0.796
Genome-wide autozygosity in Daghestan	Central Asia	Sub	122	T=0.115	G=0.885
Genome-wide autozygosity in Daghestan	Europe	Sub	108	T=0.139	G=0.861
Genome-wide autozygosity in Daghestan	South Asian	Sub	98	T=0.14	G=0.86
Genome-wide autozygosity in Daghestan	Caucasus	Sub	34	T=0.15	G=0.85
Genome of the Netherlands Release 5	Genome of the Netherlands	Study-wide	998	T=0.152	G=0.848
Northern Sweden	ACPOP	Study-wide	600	T=0.150	G=0.850
SGDP_PRJ	Global	Study-wide	516	T=0.120	G=0.880
Qatari	Global	Study-wide	216	T=0.213	G=0.787
A Vietnamese Genetic Variation Database	Global	Study-wide	216	T=0.046	G=0.954
Siberian	Global	Study-wide	54	T=0.20	G=0.80
The Danish reference pan genome	Danish	Study-wide	40	T=0.17	G=0.82
Ancient Sardinia genome-wide 1240k capture data generation and analysis	Global	Study-wide	30	T=0.20	G=0.80

Variant Details tab shows known variant placements on genomic sequences: chromosomes (NC_), RefSeqGene, pseudogenes or genomic regions (NG_), and in a separate table: on transcripts (NM_) and protein sequences (NP_). The corresponding transcript and protein locations are listed in adjacent lines, along with molecular consequences from Sequence Ontology. When no protein placement is available, only the transcript is listed. Column "Codon[Amino acid]" shows the actual base change in the format of "Reference > Alternate" allele, including the nucleotide codon change in transcripts, and the amino acid change in proteins, respectively, allowing for known ribosomal slippage sites. To view nucleotides adjacent to the variant use the Genomic View at the bottom of the page - zoom into the sequence until the nucleotides around the variant become visible.

Genomic Placements

Sequence name	Change
GRCh38.p14 chr 1	NC_000001.11:g.92469854T>G
GRCh37.p13 chr 1	NC_000001.10:g.92935411T>G

Clinical Significance tab shows a list of clinical significance entries from ClinVar associated with the variation, per allele. Click on the RCV accession (i.e. RCV000001615.2) or Allele ID (i.e. 12274) to access full ClinVar report.

Not Reported in ClinVar

Aliases tab displays HGVS names representing the variant placements and allele changes on genomic, transcript and protein sequences, per allele. HGVS name is an expression for reporting sequence accession and version, sequence type, position, and allele change. The column "Note" can have two values: "diff" means that there is a difference between the reference allele (variation interval) at the placement reported in HGVS name and the reference alleles reported in other HGVS names, and "rev" means that the sequence of this variation interval at the placement reported in HGVS name is in reverse orientation to the sequence(s) of this variation in other HGVS names not labeled as "rev".

Placement	T=	G
GRCh38.p14 chr 1	NC_000001.11:g.92469854=	NC_000001.11:g.92469854T>G
GRCh37.p13 chr 1	NC_000001.10:g.92935411=	NC_000001.10:g.92935411T>G

Submissions tab displays variations originally submitted to dbSNP, now supporting this RefSNP cluster (rs). We display Submitter handle, Submission identifier, Date and Build number, when the submission appeared for the first time. Direct submissions to dbSNP have Submission ID in the form of an ss-prefixed number (ss#). Other supporting variations are listed in the table without ss#.

132 SubSNP, 24 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	BCM_SSAHASNP	ss9820854	Jul 11, 2003 (116)
2	WI_SSAHASNP	ss14315348	Dec 05, 2003 (119)
3	SC_SNP	ss15425427	Feb 27, 2004 (120)
4	ABI	ss44058263	Mar 13, 2006 (126)
5	AFFY	ss66526460	Nov 30, 2006 (127)
6	ILLUMINA	ss66688180	Nov 30, 2006 (127)
7	ILLUMINA	ss67482221	Nov 30, 2006 (127)
8	ILLUMINA	ss67839381	Nov 30, 2006 (127)
9	ILLUMINA	ss70878293	May 25, 2008 (130)
10	ILLUMINA	ss71468438	May 17, 2007 (127)
11	ILLUMINA	ss75575943	Dec 07, 2007 (129)
12	AFFY	ss76349107	Dec 07, 2007 (129)
13	ILLUMINA	ss79228999	Dec 15, 2007 (130)
14	HGSV	ss82567915	Dec 15, 2007 (130)
15	KRIBB_YJKIM	ss84519452	Dec 15, 2007 (130)
16	BCMHGSC_JDW	ss87626000	Mar 23, 2008 (129)
17	HUMANGENOME_JCVI	ss97957987	Feb 05, 2009 (130)
18	BGI	ss106586307	Feb 05, 2009 (130)
19	1000GENOMES	ss108413991	Jan 23, 2009 (130)
20	ILLUMINA-UK	ss118889562	Dec 01, 2009 (131)
21	ILLUMINA	ss122589355	Dec 01, 2009 (131)
22	ENSEMBL	ss138036881	Dec 01, 2009 (131)
23	ENSEMBL	ss138856901	Dec 01, 2009 (131)
24	ILLUMINA	ss154373825	Dec 01, 2009 (131)
25	GMI	ss155350160	Dec 01, 2009 (131)
26	ILLUMINA	ss159549763	Dec 01, 2009 (131)
27	ILLUMINA	ss160795343	Dec 01, 2009 (131)
28	COMPLETE_GENOMICS	ss164787455	Jul 04, 2010 (132)
29	COMPLETE_GENOMICS	ss166849093	Jul 04, 2010 (132)
30	ILLUMINA	ss172167132	Jul 04, 2010 (132)
31	AFFY	ss173345758	Jul 04, 2010 (132)
32	ILLUMINA	ss174059979	Jul 04, 2010 (132)
33	BUSHMAN	ss198777293	Jul 04, 2010 (132)
34	BCM-HGSC-SUB	ss205107101	Jul 04, 2010 (132)
35	1000GENOMES	ss210587120	Jul 14, 2010 (132)
36	1000GENOMES	ss218524657	Jul 14, 2010 (132)
37	1000GENOMES	ss230637944	Jul 14, 2010 (132)
38	BL	ss253279791	May 09, 2011 (134)
39	GMI	ss275927871	May 04, 2012 (137)
40	GMI	ss284097033	Apr 25, 2013 (138)
41	PJP	ss290563721	May 09, 2011 (134)
42	ILLUMINA	ss481308881	May 04, 2012 (137)
43	ILLUMINA	ss481333956	May 04, 2012 (137)
44	ILLUMINA	ss482316266	Sep 08, 2015 (146)
45	ILLUMINA	ss485449679	May 04, 2012 (137)
46	ILLUMINA	ss537375384	Sep 08, 2015 (146)
47	SSMP	ss648220802	Apr 25, 2013 (138)
48	ILLUMINA	ss778946904	Aug 21, 2014 (142)
49	ILLUMINA	ss783170282	Aug 21, 2014 (142)
50	ILLUMINA	ss784125840	Aug 21, 2014 (142)
51	ILLUMINA	ss825559517	Apr 01, 2015 (144)
52	ILLUMINA	ss832429815	Apr 01, 2015 (144)
53	ILLUMINA	ss833060940	Aug 21, 2014 (142)
54	ILLUMINA	ss833651768	Aug 21, 2014 (142)
55	ILLUMINA	ss834408710	Aug 21, 2014 (142)
56	EVA-GONL	ss975432016	Aug 21, 2014 (142)
57	JMKIDD_LAB	ss1068091525	Aug 21, 2014 (142)
58	1000GENOMES	ss1291916700	Aug 21, 2014 (142)
59	HAMMER_LAB	ss1397253827	Sep 08, 2015 (146)
60	DDI	ss1425897073	Apr 01, 2015 (144)
61	EVA_GENOME_DK	ss1574233303	Apr 01, 2015 (144)
62	EVA_DECODE	ss1584808100	Apr 01, 2015 (144)
63	EVA_UK10K_ALSPAC	ss1600713194	Apr 01, 2015 (144)
64	EVA_UK10K_TWINSUK	ss1643707227	Apr 01, 2015 (144)
65	EVA_SVP	ss1712353390	Apr 01, 2015 (144)
66	ILLUMINA	ss1751938937	Sep 08, 2015 (146)
67	HAMMER_LAB	ss1794741674	Sep 08, 2015 (146)
68	WEILL_CORNELL_DGM	ss1918633003	Feb 12, 2016 (147)
69	GENOMED	ss1966809002	Jul 19, 2016 (147)
70	JJLAB	ss2019838192	Sep 14, 2016 (149)
71	ILLUMINA	ss2094783852	Dec 20, 2016 (150)
72	ILLUMINA	ss2094966047	Dec 20, 2016 (150)
73	USC_VALOUEV	ss2147856081	Dec 20, 2016 (150)
74	HUMAN_LONGEVITY	ss2164620109	Dec 20, 2016 (150)
75	SYSTEMSBIOZJU	ss2624430332	Nov 08, 2017 (151)
76	ILLUMINA	ss2632547691	Nov 08, 2017 (151)
77	ILLUMINA	ss2635001091	Nov 08, 2017 (151)
78	GRF	ss2697781572	Nov 08, 2017 (151)
79	GNOMAD	ss2758080030	Nov 08, 2017 (151)
80	SWEGEN	ss2987228639	Nov 08, 2017 (151)
81	BIOINF_KMB_FNS_UNIBA	ss3023681845	Nov 08, 2017 (151)
82	CSHL	ss3343574115	Nov 08, 2017 (151)
83	ILLUMINA	ss3626154792	Oct 11, 2018 (152)
84	ILLUMINA	ss3630582168	Oct 11, 2018 (152)
85	ILLUMINA	ss3632901080	Oct 11, 2018 (152)
86	ILLUMINA	ss3633595999	Oct 11, 2018 (152)
87	ILLUMINA	ss3634336627	Oct 11, 2018 (152)
88	ILLUMINA	ss3635289661	Oct 11, 2018 (152)
89	ILLUMINA	ss3636014023	Oct 11, 2018 (152)
90	ILLUMINA	ss3637040111	Oct 11, 2018 (152)
91	ILLUMINA	ss3637772191	Oct 11, 2018 (152)
92	ILLUMINA	ss3638904648	Oct 11, 2018 (152)
93	ILLUMINA	ss3639450179	Oct 11, 2018 (152)
94	ILLUMINA	ss3640043987	Oct 11, 2018 (152)
95	ILLUMINA	ss3642782751	Oct 11, 2018 (152)
96	URBANLAB	ss3646720271	Oct 11, 2018 (152)
97	ILLUMINA	ss3651439523	Oct 11, 2018 (152)
98	EGCUT_WGS	ss3655307047	Jul 12, 2019 (153)
99	EVA_DECODE	ss3687273045	Jul 12, 2019 (153)
100	ACPOP	ss3727271996	Jul 12, 2019 (153)
101	ILLUMINA	ss3744637589	Jul 12, 2019 (153)
102	EVA	ss3746515725	Jul 12, 2019 (153)
103	ILLUMINA	ss3772138858	Jul 12, 2019 (153)
104	PACBIO	ss3783482703	Jul 12, 2019 (153)
105	PACBIO	ss3789129840	Jul 12, 2019 (153)
106	PACBIO	ss3794002662	Jul 12, 2019 (153)
107	KHV_HUMAN_GENOMES	ss3799520118	Jul 12, 2019 (153)
108	EVA	ss3826303002	Apr 25, 2020 (154)
109	EVA	ss3836541770	Apr 25, 2020 (154)
110	EVA	ss3841949465	Apr 25, 2020 (154)
111	HGDP	ss3847342295	Apr 25, 2020 (154)
112	SGDP_PRJ	ss3849380252	Apr 25, 2020 (154)
113	KRGDB	ss3894445512	Apr 25, 2020 (154)
114	KOGIC	ss3945000375	Apr 25, 2020 (154)
115	EVA	ss3984812293	Apr 25, 2021 (155)
116	EVA	ss4016924767	Apr 25, 2021 (155)
117	TOPMED	ss4458929607	Apr 25, 2021 (155)
118	TOMMO_GENOMICS	ss5145095475	Apr 25, 2021 (155)
119	1000G_HIGH_COVERAGE	ss5243157875	Oct 12, 2022 (156)
120	GENOGRAPHIC	ss5314466094	Oct 12, 2022 (156)
121	EVA	ss5314634582	Oct 12, 2022 (156)
122	EVA	ss5320365902	Oct 12, 2022 (156)
123	HUGCELL_USP	ss5444125797	Oct 12, 2022 (156)
124	1000G_HIGH_COVERAGE	ss5515908605	Oct 12, 2022 (156)
125	SANFORD_IMAGENETICS	ss5626039983	Oct 12, 2022 (156)
126	TOMMO_GENOMICS	ss5670192824	Oct 12, 2022 (156)
127	EVA	ss5799491878	Oct 12, 2022 (156)
128	YY_MCH	ss5800819112	Oct 12, 2022 (156)
129	EVA	ss5832306248	Oct 12, 2022 (156)
130	EVA	ss5849014208	Oct 12, 2022 (156)
131	EVA	ss5909282487	Oct 12, 2022 (156)
132	EVA	ss5937894237	Oct 12, 2022 (156)
133	1000Genomes	NC_000001.10 - 92935411	Oct 11, 2018 (152)
134	1000Genomes_30x	NC_000001.11 - 92469854	Oct 12, 2022 (156)
135	The Avon Longitudinal Study of Parents and Children	NC_000001.10 - 92935411	Oct 11, 2018 (152)
136	Genome-wide autozygosity in Daghestan	NC_000001.9 - 92707999	Apr 25, 2020 (154)
137	Genetic variation in the Estonian population	NC_000001.10 - 92935411	Oct 11, 2018 (152)
138	Genographic Project	NC_000001.11 - 92469854	Oct 12, 2022 (156)
139	The Danish reference pan genome	NC_000001.10 - 92935411	Apr 25, 2020 (154)
140	gnomAD - Genomes	NC_000001.11 - 92469854	Apr 25, 2021 (155)
141	Genome of the Netherlands Release 5	NC_000001.10 - 92935411	Apr 25, 2020 (154)
142	HGDP-CEPH-db Supplement 1	NC_000001.9 - 92707999	Apr 25, 2020 (154)
143	HapMap	NC_000001.11 - 92469854	Apr 25, 2020 (154)
144	KOREAN population from KRGDB	NC_000001.10 - 92935411	Apr 25, 2020 (154)
145	Korean Genome Project	NC_000001.11 - 92469854	Apr 25, 2020 (154)
146	Northern Sweden	NC_000001.10 - 92935411	Jul 12, 2019 (153)
147	Ancient Sardinia genome-wide 1240k capture data generation and analysis	NC_000001.10 - 92935411	Apr 25, 2021 (155)
148	Qatari	NC_000001.10 - 92935411	Apr 25, 2020 (154)
149	SGDP_PRJ	NC_000001.10 - 92935411	Apr 25, 2020 (154)
150	Siberian	NC_000001.10 - 92935411	Apr 25, 2020 (154)
151	8.3KJPN	NC_000001.10 - 92935411	Apr 25, 2021 (155)
152	14KJPN	NC_000001.11 - 92469854	Oct 12, 2022 (156)
153	TopMed	NC_000001.11 - 92469854	Apr 25, 2021 (155)
154	UK 10K study - Twins	NC_000001.10 - 92935411	Oct 11, 2018 (152)
155	A Vietnamese Genetic Variation Database	NC_000001.10 - 92935411	Jul 12, 2019 (153)
156	ALFA	NC_000001.11 - 92469854	Apr 25, 2021 (155)

History tab displays RefSNPs (Associated ID) from previous builds (Build) that now support the current RefSNP, and the dates, when the history was updated for each Associated ID (History Updated).

Associated ID	History Updated (Build)
rs59080612	May 25, 2008 (130)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss82567915, ss3638904648, ss3639450179	NC_000001.8:92647431:T:G	NC_000001.11:92469853:T:G	(self)
15144, 20187, ss66526460, ss76349107, ss87626000, ss108413991, ss118889562, ss160795343, ss164787455, ss166849093, ss173345758, ss198777293, ss205107101, ss210587120, ss253279791, ss275927871, ss284097033, ss290563721, ss481308881, ss825559517, ss1397253827, ss1584808100, ss1712353390, ss2635001091, ss3642782751, ss3847342295	NC_000001.9:92707998:T:G	NC_000001.11:92469853:T:G	(self)
2673385, 1470073, 1045295, 1608989, 637214, 1622906, 556861, 38220, 674933, 1397232, 372435, 3064782, 1470073, 315992, ss218524657, ss230637944, ss481333956, ss482316266, ss485449679, ss537375384, ss648220802, ss778946904, ss783170282, ss784125840, ss832429815, ss833060940, ss833651768, ss834408710, ss975432016, ss1068091525, ss1291916700, ss1425897073, ss1574233303, ss1600713194, ss1643707227, ss1751938937, ss1794741674, ss1918633003, ss1966809002, ss2019838192, ss2094783852, ss2094966047, ss2147856081, ss2624430332, ss2632547691, ss2697781572, ss2758080030, ss2987228639, ss3343574115, ss3626154792, ss3630582168, ss3632901080, ss3633595999, ss3634336627, ss3635289661, ss3636014023, ss3637040111, ss3637772191, ss3640043987, ss3651439523, ss3655307047, ss3727271996, ss3744637589, ss3746515725, ss3772138858, ss3783482703, ss3789129840, ss3794002662, ss3826303002, ss3836541770, ss3849380252, ss3894445512, ss3984812293, ss4016924767, ss5145095475, ss5314634582, ss5320365902, ss5626039983, ss5799491878, ss5832306248, ss5937894237	NC_000001.10:92935410:T:G	NC_000001.11:92469853:T:G	(self)
3434540, 64326, 18866502, 126720, 1378376, 4029928, 22535942, 2853113109, ss2164620109, ss3023681845, ss3646720271, ss3687273045, ss3799520118, ss3841949465, ss3945000375, ss4458929607, ss5243157875, ss5314466094, ss5444125797, ss5515908605, ss5670192824, ss5800819112, ss5849014208, ss5909282487	NC_000001.11:92469853:T:G	NC_000001.11:92469853:T:G	(self)
ss14315348, ss15425427	NT_028050.13:1133232:T:G	NC_000001.11:92469853:T:G	(self)
ss44058263, ss66688180, ss67482221, ss67839381, ss70878293, ss71468438, ss75575943, ss79228999, ss84519452, ss97957987, ss106586307, ss122589355, ss138036881, ss138856901, ss154373825, ss155350160, ss159549763, ss172167132, ss174059979	NT_032977.9:62907328:T:G	NC_000001.11:92469853:T:G	(self)
ss9820854	NT_077927.1:1135232:T:G	NC_000001.11:92469853:T:G	(self)

Publications tab displays PubMed articles citing the variation as a listing of PMID, Title, Author, Year, Journal, ordered by Year, descending.

2 citations for rs6662618

PMID	Title	Author	Year	Journal
20075157	A variant allele of Growth Factor Independence 1 (GFI1) is associated with acute myeloid leukemia.	Khandanpour C et al.	2010	Blood
27490719	Literature-Informed Analysis of a Genome-Wide Association Study of Gestational Age in Norwegian Women and Children Suggests Involvement of Inflammatory Pathways.	Bacelis J et al.	2016	PloS one

The Flanks tab provides retrieving flanking sequences of a SNP on all molecules that have placements.

Genome context:

Select flank length:

Genomic regions, transcripts, and products
Top▲ Help
NCBI Graphical Sequence Viewer display of the genomic region, transcripts and protein products for the reported RefSNP (rs).
Use the zoom option to view the nucleotides around the RefSNP and find other neighboring RefSNPs.
Visit Sequence Viewer for help with navigating inside the display and modifying the selection of displayed data tracks.

Choose placement

dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs6662618