Name: rs9394274
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.

rs9394274

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr6:35147134 (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: A>C / A>G / A>T
Variation Type: SNV Single Nucleotide Variation
Frequency: A=0.443277 (117331/264690, TOPMED)
A=0.326608 (44467/136148, ALFA)
A=0.33824 (9558/28258, 14KJPN) (+ 19 more)
A=0.33801 (5665/16760, 8.3KJPN)
A=0.4678 (2996/6404, 1000G_30x)
A=0.4631 (2319/5008, 1000G)
A=0.2074 (929/4480, Estonian)
A=0.2862 (1103/3854, ALSPAC)
A=0.3007 (1115/3708, TWINSUK)
A=0.3625 (1062/2930, KOREAN)
A=0.3934 (819/2082, HGDP_Stanford)
C=0.4794 (906/1890, HapMap)
A=0.3630 (665/1832, Korea1K)
A=0.2861 (325/1136, Daghestan)
A=0.281 (280/998, GoNL)
A=0.208 (125/600, NorthernSweden)
A=0.259 (115/444, SGDP_PRJ)
A=0.435 (94/216, Qatari)
C=0.472 (101/214, Vietnamese)
A=0.32 (18/56, Ancient Sardinia)
A=0.21 (12/56, Siberian)
A=0.23 (9/40, GENOME_DK)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: None
Publications: 0 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	136148	A=0.326608	C=0.673392, G=0.000000, T=0.000000	0.126612	0.473397	0.399991	32
European	Sub	119246	A=0.292328	C=0.707672, G=0.000000, T=0.000000	0.08916	0.504503	0.406336	11
African	Sub	8122	A=0.8019	C=0.1981, G=0.0000, T=0.0000	0.655011	0.051219	0.29377	13
African Others	Sub	294	A=0.864	C=0.136, G=0.000, T=0.000	0.741497	0.013605	0.244898	0
African American	Sub	7828	A=0.7996	C=0.2004, G=0.0000, T=0.0000	0.651763	0.052632	0.295606	13
Asian	Sub	556	A=0.466	C=0.534, G=0.000, T=0.000	0.255396	0.323741	0.420863	4
East Asian	Sub	434	A=0.438	C=0.562, G=0.000, T=0.000	0.239631	0.364055	0.396313	5
Other Asian	Sub	122	A=0.566	C=0.434, G=0.000, T=0.000	0.311475	0.180328	0.508197	0
Latin American 1	Sub	562	A=0.374	C=0.626, G=0.000, T=0.000	0.131673	0.384342	0.483986	0
Latin American 2	Sub	1682	A=0.2551	C=0.7449, G=0.0000, T=0.0000	0.0761	0.565993	0.357907	2
South Asian	Sub	104	A=0.375	C=0.625, G=0.000, T=0.000	0.153846	0.403846	0.442308	0
Other	Sub	5876	A=0.3673	C=0.6327, G=0.0000, T=0.0000	0.15759	0.423077	0.419333	15

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").

Download

Study	Population	Group	Sample Size	Ref Allele	Alt Allele
TopMed	Global	Study-wide	264690	A=0.443277	C=0.556723
Allele Frequency Aggregator	Total	Global	136148	A=0.326608	C=0.673392, G=0.000000, T=0.000000
Allele Frequency Aggregator	European	Sub	119246	A=0.292328	C=0.707672, G=0.000000, T=0.000000
Allele Frequency Aggregator	African	Sub	8122	A=0.8019	C=0.1981, G=0.0000, T=0.0000
Allele Frequency Aggregator	Other	Sub	5876	A=0.3673	C=0.6327, G=0.0000, T=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	1682	A=0.2551	C=0.7449, G=0.0000, T=0.0000
Allele Frequency Aggregator	Latin American 1	Sub	562	A=0.374	C=0.626, G=0.000, T=0.000
Allele Frequency Aggregator	Asian	Sub	556	A=0.466	C=0.534, G=0.000, T=0.000
Allele Frequency Aggregator	South Asian	Sub	104	A=0.375	C=0.625, G=0.000, T=0.000
14KJPN	JAPANESE	Study-wide	28258	A=0.33824	C=0.66176
8.3KJPN	JAPANESE	Study-wide	16760	A=0.33801	C=0.66199
1000Genomes_30x	Global	Study-wide	6404	A=0.4678	C=0.5322
1000Genomes_30x	African	Sub	1786	A=0.8191	C=0.1809
1000Genomes_30x	Europe	Sub	1266	A=0.2907	C=0.7093
1000Genomes_30x	South Asian	Sub	1202	A=0.3128	C=0.6872
1000Genomes_30x	East Asian	Sub	1170	A=0.4479	C=0.5521
1000Genomes_30x	American	Sub	980	A=0.270	C=0.730
1000Genomes	Global	Study-wide	5008	A=0.4631	C=0.5369
1000Genomes	African	Sub	1322	A=0.8147	C=0.1853
1000Genomes	East Asian	Sub	1008	A=0.4425	C=0.5575
1000Genomes	Europe	Sub	1006	A=0.2813	C=0.7187
1000Genomes	South Asian	Sub	978	A=0.327	C=0.673
1000Genomes	American	Sub	694	A=0.278	C=0.722
Genetic variation in the Estonian population	Estonian	Study-wide	4480	A=0.2074	C=0.7926
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	A=0.2862	C=0.7138
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	A=0.3007	C=0.6993
KOREAN population from KRGDB	KOREAN	Study-wide	2930	A=0.3625	C=0.6375
HGDP-CEPH-db Supplement 1	Global	Study-wide	2082	A=0.3934	C=0.6066
HGDP-CEPH-db Supplement 1	Est_Asia	Sub	470	A=0.387	C=0.613
HGDP-CEPH-db Supplement 1	Central_South_Asia	Sub	414	A=0.357	C=0.643
HGDP-CEPH-db Supplement 1	Middle_Est	Sub	348	A=0.359	C=0.641
HGDP-CEPH-db Supplement 1	Europe	Sub	320	A=0.294	C=0.706
HGDP-CEPH-db Supplement 1	Africa	Sub	242	A=0.818	C=0.182
HGDP-CEPH-db Supplement 1	America	Sub	216	A=0.037	C=0.963
HGDP-CEPH-db Supplement 1	Oceania	Sub	72	A=0.89	C=0.11
HapMap	Global	Study-wide	1890	A=0.5206	C=0.4794
HapMap	American	Sub	768	A=0.379	C=0.621
HapMap	African	Sub	692	A=0.777	C=0.223
HapMap	Asian	Sub	254	A=0.406	C=0.594
HapMap	Europe	Sub	176	A=0.295	C=0.705
Korean Genome Project	KOREAN	Study-wide	1832	A=0.3630	C=0.6370
Genome-wide autozygosity in Daghestan	Global	Study-wide	1136	A=0.2861	C=0.7139
Genome-wide autozygosity in Daghestan	Daghestan	Sub	628	A=0.261	C=0.739
Genome-wide autozygosity in Daghestan	Near_East	Sub	144	A=0.347	C=0.653
Genome-wide autozygosity in Daghestan	Central Asia	Sub	122	A=0.221	C=0.779
Genome-wide autozygosity in Daghestan	Europe	Sub	108	A=0.343	C=0.657
Genome-wide autozygosity in Daghestan	South Asian	Sub	98	A=0.38	C=0.62
Genome-wide autozygosity in Daghestan	Caucasus	Sub	36	A=0.28	C=0.72
Genome of the Netherlands Release 5	Genome of the Netherlands	Study-wide	998	A=0.281	C=0.719
Northern Sweden	ACPOP	Study-wide	600	A=0.208	C=0.792
SGDP_PRJ	Global	Study-wide	444	A=0.259	C=0.741
Qatari	Global	Study-wide	216	A=0.435	C=0.565
A Vietnamese Genetic Variation Database	Global	Study-wide	214	A=0.528	C=0.472
Ancient Sardinia genome-wide 1240k capture data generation and analysis	Global	Study-wide	56	A=0.32	C=0.68
Siberian	Global	Study-wide	56	A=0.21	C=0.79
The Danish reference pan genome	Danish	Study-wide	40	A=0.23	C=0.78

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 6	NC_000006.12:g.35147134A>C
GRCh38.p14 chr 6	NC_000006.12:g.35147134A>G
GRCh38.p14 chr 6	NC_000006.12:g.35147134A>T
GRCh37.p13 chr 6	NC_000006.11:g.35114911A>C
GRCh37.p13 chr 6	NC_000006.11:g.35114911A>G
GRCh37.p13 chr 6	NC_000006.11:g.35114911A>T

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	A=	C	G	T
GRCh38.p14 chr 6	NC_000006.12:g.35147134=	NC_000006.12:g.35147134A>C	NC_000006.12:g.35147134A>G	NC_000006.12:g.35147134A>T
GRCh37.p13 chr 6	NC_000006.11:g.35114911=	NC_000006.11:g.35114911A>C	NC_000006.11:g.35114911A>G	NC_000006.11:g.35114911A>T

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#.

113 SubSNP, 24 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	SC_SNP	ss12895848	Dec 05, 2003 (119)
2	SSAHASNP	ss22406868	Apr 05, 2004 (121)
3	PERLEGEN	ss23941042	Sep 20, 2004 (123)
4	ABI	ss44697362	Mar 14, 2006 (126)
5	ILLUMINA	ss68040707	Nov 29, 2006 (127)
6	ILLUMINA	ss71605378	May 16, 2007 (127)
7	ILLUMINA	ss75382177	Dec 07, 2007 (129)
8	HGSV	ss83161578	Dec 14, 2007 (130)
9	BCMHGSC_JDW	ss93442332	Mar 24, 2008 (129)
10	HUMANGENOME_JCVI	ss98490118	Feb 04, 2009 (130)
11	BGI	ss104302537	Dec 01, 2009 (131)
12	1000GENOMES	ss109944514	Jan 24, 2009 (130)
13	1000GENOMES	ss114201636	Jan 25, 2009 (130)
14	KRIBB_YJKIM	ss119591221	Dec 01, 2009 (131)
15	ENSEMBL	ss143066036	Dec 01, 2009 (131)
16	ENSEMBL	ss143836096	Dec 01, 2009 (131)
17	GMI	ss156798744	Dec 01, 2009 (131)
18	ILLUMINA	ss160984316	Dec 01, 2009 (131)
19	COMPLETE_GENOMICS	ss162240726	Jul 04, 2010 (132)
20	COMPLETE_GENOMICS	ss163395796	Jul 04, 2010 (132)
21	ILLUMINA	ss174834996	Jul 04, 2010 (132)
22	BUSHMAN	ss201680447	Jul 04, 2010 (132)
23	BCM-HGSC-SUB	ss207652145	Jul 04, 2010 (132)
24	1000GENOMES	ss222331196	Jul 14, 2010 (132)
25	1000GENOMES	ss233427065	Jul 14, 2010 (132)
26	1000GENOMES	ss240492623	Jul 15, 2010 (132)
27	GMI	ss278752024	May 04, 2012 (137)
28	GMI	ss285385589	Apr 25, 2013 (138)
29	PJP	ss293836376	May 09, 2011 (134)
30	ILLUMINA	ss410957815	Sep 17, 2011 (135)
31	ILLUMINA	ss481890054	May 04, 2012 (137)
32	ILLUMINA	ss481923128	May 04, 2012 (137)
33	ILLUMINA	ss482881465	Sep 08, 2015 (146)
34	ILLUMINA	ss485739155	May 04, 2012 (137)
35	ILLUMINA	ss537595040	Sep 08, 2015 (146)
36	TISHKOFF	ss559134834	Apr 25, 2013 (138)
37	SSMP	ss653070423	Apr 25, 2013 (138)
38	ILLUMINA	ss779009163	Aug 21, 2014 (142)
39	ILLUMINA	ss783315329	Aug 21, 2014 (142)
40	ILLUMINA	ss784267366	Aug 21, 2014 (142)
41	ILLUMINA	ss832576838	Apr 01, 2015 (144)
42	ILLUMINA	ss834471618	Aug 21, 2014 (142)
43	EVA-GONL	ss982810824	Aug 21, 2014 (142)
44	JMKIDD_LAB	ss1073528091	Aug 21, 2014 (142)
45	1000GENOMES	ss1319671565	Aug 21, 2014 (142)
46	HAMMER_LAB	ss1397453311	Sep 08, 2015 (146)
47	DDI	ss1430686913	Apr 01, 2015 (144)
48	EVA_GENOME_DK	ss1581625688	Apr 01, 2015 (144)
49	EVA_DECODE	ss1592343940	Apr 01, 2015 (144)
50	EVA_UK10K_ALSPAC	ss1615332298	Apr 01, 2015 (144)
51	EVA_UK10K_TWINSUK	ss1658326331	Apr 01, 2015 (144)
52	EVA_SVP	ss1712854679	Apr 01, 2015 (144)
53	ILLUMINA	ss1752633734	Sep 08, 2015 (146)
54	HAMMER_LAB	ss1804378180	Sep 08, 2015 (146)
55	WEILL_CORNELL_DGM	ss1926067775	Feb 12, 2016 (147)
56	GENOMED	ss1970370320	Jul 19, 2016 (147)
57	JJLAB	ss2023671139	Sep 14, 2016 (149)
58	ILLUMINA	ss2094957220	Dec 20, 2016 (150)
59	ILLUMINA	ss2095182554	Dec 20, 2016 (150)
60	USC_VALOUEV	ss2151848529	Dec 20, 2016 (150)
61	HUMAN_LONGEVITY	ss2283134302	Dec 20, 2016 (150)
62	SYSTEMSBIOZJU	ss2626323860	Nov 08, 2017 (151)
63	ILLUMINA	ss2634438318	Nov 08, 2017 (151)
64	GRF	ss2707444385	Nov 08, 2017 (151)
65	GNOMAD	ss2837715874	Nov 08, 2017 (151)
66	SWEGEN	ss2998879269	Nov 08, 2017 (151)
67	BIOINF_KMB_FNS_UNIBA	ss3025627656	Nov 08, 2017 (151)
68	CSHL	ss3346909697	Nov 08, 2017 (151)
69	ILLUMINA	ss3629521047	Oct 12, 2018 (152)
70	ILLUMINA	ss3632355838	Oct 12, 2018 (152)
71	ILLUMINA	ss3633418107	Oct 12, 2018 (152)
72	ILLUMINA	ss3634140807	Oct 12, 2018 (152)
73	ILLUMINA	ss3635061987	Oct 12, 2018 (152)
74	ILLUMINA	ss3635821709	Oct 12, 2018 (152)
75	ILLUMINA	ss3636784602	Oct 12, 2018 (152)
76	ILLUMINA	ss3637574510	Oct 12, 2018 (152)
77	ILLUMINA	ss3638623989	Oct 12, 2018 (152)
78	ILLUMINA	ss3640769286	Oct 12, 2018 (152)
79	ILLUMINA	ss3643565485	Oct 12, 2018 (152)
80	URBANLAB	ss3648327670	Oct 12, 2018 (152)
81	ILLUMINA	ss3653126344	Oct 12, 2018 (152)
82	EGCUT_WGS	ss3666766257	Jul 13, 2019 (153)
83	EVA_DECODE	ss3716983128	Jul 13, 2019 (153)
84	ACPOP	ss3733403588	Jul 13, 2019 (153)
85	ILLUMINA	ss3745361923	Jul 13, 2019 (153)
86	EVA	ss3764876835	Jul 13, 2019 (153)
87	ILLUMINA	ss3772855564	Jul 13, 2019 (153)
88	KHV_HUMAN_GENOMES	ss3808029962	Jul 13, 2019 (153)
89	EVA	ss3829864698	Apr 26, 2020 (154)
90	EVA	ss3838409790	Apr 26, 2020 (154)
91	EVA	ss3843853900	Apr 26, 2020 (154)
92	HGDP	ss3847830380	Apr 26, 2020 (154)
93	SGDP_PRJ	ss3864345840	Apr 26, 2020 (154)
94	KRGDB	ss3911129648	Apr 26, 2020 (154)
95	KOGIC	ss3958792108	Apr 26, 2020 (154)
96	EVA	ss3985216559	Apr 26, 2021 (155)
97	TOPMED	ss4699132416	Apr 26, 2021 (155)
98	TOMMO_GENOMICS	ss5176995375	Apr 26, 2021 (155)
99	1000G_HIGH_COVERAGE	ss5268042175	Oct 13, 2022 (156)
100	EVA	ss5315148028	Oct 13, 2022 (156)
101	EVA	ss5364892124	Oct 13, 2022 (156)
102	HUGCELL_USP	ss5465754681	Oct 13, 2022 (156)
103	EVA	ss5508450056	Oct 13, 2022 (156)
104	1000G_HIGH_COVERAGE	ss5553743227	Oct 13, 2022 (156)
105	SANFORD_IMAGENETICS	ss5640172511	Oct 13, 2022 (156)
106	TOMMO_GENOMICS	ss5714891772	Oct 13, 2022 (156)
107	EVA	ss5799685850	Oct 13, 2022 (156)
108	YY_MCH	ss5807367814	Oct 13, 2022 (156)
109	EVA	ss5842082279	Oct 13, 2022 (156)
110	EVA	ss5855309150	Oct 13, 2022 (156)
111	EVA	ss5883352414	Oct 13, 2022 (156)
112	EVA	ss5968661600	Oct 13, 2022 (156)
113	EVA	ss5980361723	Oct 13, 2022 (156)
114	1000Genomes	NC_000006.11 - 35114911	Oct 12, 2018 (152)
115	1000Genomes_30x	NC_000006.12 - 35147134	Oct 13, 2022 (156)
116	The Avon Longitudinal Study of Parents and Children	NC_000006.11 - 35114911	Oct 12, 2018 (152)
117	Genome-wide autozygosity in Daghestan	NC_000006.10 - 35222889	Apr 26, 2020 (154)
118	Genetic variation in the Estonian population	NC_000006.11 - 35114911	Oct 12, 2018 (152)
119	The Danish reference pan genome	NC_000006.11 - 35114911	Apr 26, 2020 (154)
120	gnomAD - Genomes Submission ignored due to conflicting rows: Row 221921407 (NC_000006.12:35147133:A:C 80609/140048) Row 221921408 (NC_000006.12:35147133:A:G 3/140098)	-	Apr 26, 2021 (155)
121	gnomAD - Genomes Submission ignored due to conflicting rows: Row 221921407 (NC_000006.12:35147133:A:C 80609/140048) Row 221921408 (NC_000006.12:35147133:A:G 3/140098)	-	Apr 26, 2021 (155)
122	Genome of the Netherlands Release 5	NC_000006.11 - 35114911	Apr 26, 2020 (154)
123	HGDP-CEPH-db Supplement 1	NC_000006.10 - 35222889	Apr 26, 2020 (154)
124	HapMap	NC_000006.12 - 35147134	Apr 26, 2020 (154)
125	KOREAN population from KRGDB	NC_000006.11 - 35114911	Apr 26, 2020 (154)
126	Korean Genome Project	NC_000006.12 - 35147134	Apr 26, 2020 (154)
127	Northern Sweden	NC_000006.11 - 35114911	Jul 13, 2019 (153)
128	Ancient Sardinia genome-wide 1240k capture data generation and analysis	NC_000006.11 - 35114911	Apr 26, 2021 (155)
129	Qatari	NC_000006.11 - 35114911	Apr 26, 2020 (154)
130	SGDP_PRJ	NC_000006.11 - 35114911	Apr 26, 2020 (154)
131	Siberian	NC_000006.11 - 35114911	Apr 26, 2020 (154)
132	8.3KJPN	NC_000006.11 - 35114911	Apr 26, 2021 (155)
133	14KJPN	NC_000006.12 - 35147134	Oct 13, 2022 (156)
134	TopMed	NC_000006.12 - 35147134	Apr 26, 2021 (155)
135	UK 10K study - Twins	NC_000006.11 - 35114911	Oct 12, 2018 (152)
136	A Vietnamese Genetic Variation Database	NC_000006.11 - 35114911	Jul 13, 2019 (153)
137	ALFA	NC_000006.12 - 35147134	Apr 26, 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)
rs57649788	May 24, 2008 (130)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss83161578	NC_000006.9:35222888:A:C	NC_000006.12:35147133:A:C	(self)
427955, 508272, ss93442332, ss109944514, ss114201636, ss160984316, ss162240726, ss163395796, ss201680447, ss207652145, ss278752024, ss285385589, ss293836376, ss410957815, ss481890054, ss1397453311, ss1592343940, ss1712854679, ss2094957220, ss3643565485, ss3847830380	NC_000006.10:35222888:A:C	NC_000006.12:35147133:A:C	(self)
31443465, 17528302, 12504505, 7790627, 7804014, 18307042, 6688453, 442486, 8109705, 16362820, 4364883, 34964682, 17528302, 3892580, ss222331196, ss233427065, ss240492623, ss481923128, ss482881465, ss485739155, ss537595040, ss559134834, ss653070423, ss779009163, ss783315329, ss784267366, ss832576838, ss834471618, ss982810824, ss1073528091, ss1319671565, ss1430686913, ss1581625688, ss1615332298, ss1658326331, ss1752633734, ss1804378180, ss1926067775, ss1970370320, ss2023671139, ss2095182554, ss2151848529, ss2626323860, ss2634438318, ss2707444385, ss2837715874, ss2998879269, ss3346909697, ss3629521047, ss3632355838, ss3633418107, ss3634140807, ss3635061987, ss3635821709, ss3636784602, ss3637574510, ss3638623989, ss3640769286, ss3653126344, ss3666766257, ss3733403588, ss3745361923, ss3764876835, ss3772855564, ss3829864698, ss3838409790, ss3864345840, ss3911129648, ss3985216559, ss5176995375, ss5315148028, ss5364892124, ss5508450056, ss5640172511, ss5799685850, ss5842082279, ss5968661600, ss5980361723	NC_000006.11:35114910:A:C	NC_000006.12:35147133:A:C	(self)
41269162, 3107758, 15170109, 48728876, 536509974, 5873431274, ss2283134302, ss3025627656, ss3648327670, ss3716983128, ss3808029962, ss3843853900, ss3958792108, ss4699132416, ss5268042175, ss5465754681, ss5553743227, ss5714891772, ss5807367814, ss5855309150, ss5883352414	NC_000006.12:35147133:A:C	NC_000006.12:35147133:A:C	(self)
ss12895848, ss22406868	NT_007592.13:25912037:A:C	NC_000006.12:35147133:A:C	(self)
ss23941042, ss44697362, ss68040707, ss71605378, ss75382177, ss98490118, ss104302537, ss119591221, ss143066036, ss143836096, ss156798744, ss174834996	NT_007592.15:35054910:A:C	NC_000006.12:35147133:A:C	(self)
5873431274	NC_000006.12:35147133:A:G	NC_000006.12:35147133:A:G	(self)
5873431274	NC_000006.12:35147133:A:T	NC_000006.12:35147133:A:T	(self)

Removed from this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Destination RSIDs
ss2451515938	NC_000006.11:35114910:A:T	NC_000006.12:35147133:A:T

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

No publications for rs9394274

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

rs9394274