Name: rs1194
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.

rs1194

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr6:35295778 (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
Variation Type: SNV Single Nucleotide Variation
Frequency: A=0.227700 (60270/264690, TOPMED)
A=0.217214 (30416/140028, GnomAD)
A=0.17623 (10452/59310, ALFA) (+ 17 more)
A=0.33456 (9454/28258, 14KJPN)
A=0.33496 (5614/16760, 8.3KJPN)
A=0.2562 (1641/6404, 1000G_30x)
A=0.2548 (1276/5008, 1000G)
A=0.1069 (479/4480, Estonian)
A=0.1596 (615/3854, ALSPAC)
A=0.1578 (585/3708, TWINSUK)
A=0.2976 (872/2930, KOREAN)
A=0.2873 (543/1890, HapMap)
A=0.134 (134/998, GoNL)
A=0.147 (88/600, NorthernSweden)
A=0.212 (113/534, MGP)
A=0.170 (90/528, SGDP_PRJ)
A=0.241 (52/216, Qatari)
A=0.321 (68/212, Vietnamese)
A=0.09 (5/56, Siberian)
A=0.07 (3/40, GENOME_DK)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: ZNF76 : 3 Prime UTR Variant
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	59310	A=0.17623	G=0.82377	0.035576	0.683123	0.281302	16
European	Sub	43518	A=0.15074	G=0.84926	0.02399	0.722506	0.253504	1
African	Sub	5160	A=0.3403	G=0.6597	0.121705	0.441085	0.437209	1
African Others	Sub	190	A=0.311	G=0.689	0.115789	0.494737	0.389474	0
African American	Sub	4970	A=0.3414	G=0.6586	0.121932	0.439034	0.439034	1
Asian	Sub	454	A=0.313	G=0.687	0.101322	0.475771	0.422907	0
East Asian	Sub	386	A=0.326	G=0.674	0.11399	0.46114	0.42487	0
Other Asian	Sub	68	A=0.24	G=0.76	0.029412	0.558824	0.411765	0
Latin American 1	Sub	596	A=0.210	G=0.790	0.026846	0.607383	0.365772	2
Latin American 2	Sub	4982	A=0.1941	G=0.8059	0.034524	0.646327	0.319149	1
South Asian	Sub	178	A=0.152	G=0.848	0.033708	0.730337	0.235955	0
Other	Sub	4422	A=0.1979	G=0.8021	0.044776	0.649028	0.306196	2

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	A=0.227700	G=0.772300
gnomAD - Genomes	Global	Study-wide	140028	A=0.217214	G=0.782786
gnomAD - Genomes	European	Sub	75872	A=0.14700	G=0.85300
gnomAD - Genomes	African	Sub	41908	A=0.34368	G=0.65632
gnomAD - Genomes	American	Sub	13660	A=0.16720	G=0.83280
gnomAD - Genomes	Ashkenazi Jewish	Sub	3316	A=0.3405	G=0.6595
gnomAD - Genomes	East Asian	Sub	3120	A=0.3135	G=0.6865
gnomAD - Genomes	Other	Sub	2152	A=0.2179	G=0.7821
Allele Frequency Aggregator	Total	Global	59310	A=0.17623	G=0.82377
Allele Frequency Aggregator	European	Sub	43518	A=0.15074	G=0.84926
Allele Frequency Aggregator	African	Sub	5160	A=0.3403	G=0.6597
Allele Frequency Aggregator	Latin American 2	Sub	4982	A=0.1941	G=0.8059
Allele Frequency Aggregator	Other	Sub	4422	A=0.1979	G=0.8021
Allele Frequency Aggregator	Latin American 1	Sub	596	A=0.210	G=0.790
Allele Frequency Aggregator	Asian	Sub	454	A=0.313	G=0.687
Allele Frequency Aggregator	South Asian	Sub	178	A=0.152	G=0.848
14KJPN	JAPANESE	Study-wide	28258	A=0.33456	G=0.66544
8.3KJPN	JAPANESE	Study-wide	16760	A=0.33496	G=0.66504
1000Genomes_30x	Global	Study-wide	6404	A=0.2562	G=0.7438
1000Genomes_30x	African	Sub	1786	A=0.3819	G=0.6181
1000Genomes_30x	Europe	Sub	1266	A=0.1532	G=0.8468
1000Genomes_30x	South Asian	Sub	1202	A=0.1464	G=0.8536
1000Genomes_30x	East Asian	Sub	1170	A=0.3299	G=0.6701
1000Genomes_30x	American	Sub	980	A=0.207	G=0.793
1000Genomes	Global	Study-wide	5008	A=0.2548	G=0.7452
1000Genomes	African	Sub	1322	A=0.3797	G=0.6203
1000Genomes	East Asian	Sub	1008	A=0.3393	G=0.6607
1000Genomes	Europe	Sub	1006	A=0.1521	G=0.8479
1000Genomes	South Asian	Sub	978	A=0.142	G=0.858
1000Genomes	American	Sub	694	A=0.202	G=0.798
Genetic variation in the Estonian population	Estonian	Study-wide	4480	A=0.1069	G=0.8931
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	A=0.1596	G=0.8404
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	A=0.1578	G=0.8422
KOREAN population from KRGDB	KOREAN	Study-wide	2930	A=0.2976	C=0.0000, G=0.7024
HapMap	Global	Study-wide	1890	A=0.2873	G=0.7127
HapMap	American	Sub	768	A=0.199	G=0.801
HapMap	African	Sub	692	A=0.376	G=0.624
HapMap	Asian	Sub	254	A=0.386	G=0.614
HapMap	Europe	Sub	176	A=0.182	G=0.818
Genome of the Netherlands Release 5	Genome of the Netherlands	Study-wide	998	A=0.134	G=0.866
Northern Sweden	ACPOP	Study-wide	600	A=0.147	G=0.853
Medical Genome Project healthy controls from Spanish population	Spanish controls	Study-wide	534	A=0.212	G=0.788
SGDP_PRJ	Global	Study-wide	528	A=0.170	G=0.830
Qatari	Global	Study-wide	216	A=0.241	G=0.759
A Vietnamese Genetic Variation Database	Global	Study-wide	212	A=0.321	G=0.679
Siberian	Global	Study-wide	56	A=0.09	G=0.91
The Danish reference pan genome	Danish	Study-wide	40	A=0.07	G=0.93

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.35295778A>C
GRCh38.p14 chr 6	NC_000006.12:g.35295778A>G
GRCh37.p13 chr 6	NC_000006.11:g.35263555A>C
GRCh37.p13 chr 6	NC_000006.11:g.35263555A>G

Gene: ZNF76, zinc finger protein 76 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
ZNF76 transcript variant 1	NM_003427.5:c.*530=	N/A	3 Prime UTR Variant
ZNF76 transcript variant 2	NM_001292032.2:c.*530=	N/A	3 Prime UTR Variant
ZNF76 transcript variant X3	XM_017011249.3:c.*530=	N/A	3 Prime UTR Variant
ZNF76 transcript variant X5	XM_047419302.1:c.*530=	N/A	3 Prime UTR Variant
ZNF76 transcript variant X10	XM_017011255.2:c.*530=	N/A	3 Prime UTR Variant
ZNF76 transcript variant X11	XM_017011256.2:c.*530=	N/A	3 Prime UTR Variant
ZNF76 transcript variant X9	XM_011514856.4:c.	N/A	Genic Downstream Transcript Variant
ZNF76 transcript variant X1	XM_047419299.1:c.	N/A	Genic Downstream Transcript Variant
ZNF76 transcript variant X2	XM_047419300.1:c.	N/A	Genic Downstream Transcript Variant
ZNF76 transcript variant X4	XM_047419301.1:c.	N/A	Genic Downstream Transcript Variant
ZNF76 transcript variant X6	XM_047419303.1:c.	N/A	Genic Downstream Transcript Variant
ZNF76 transcript variant X7	XM_047419304.1:c.	N/A	Genic Downstream Transcript Variant
ZNF76 transcript variant X8	XM_047419305.1:c.	N/A	Genic Downstream Transcript Variant
ZNF76 transcript variant X12	XM_047419306.1:c.	N/A	Genic Downstream Transcript Variant
ZNF76 transcript variant X13	XM_047419307.1:c.	N/A	Genic Downstream Transcript Variant

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
GRCh38.p14 chr 6	NC_000006.12:g.35295778=	NC_000006.12:g.35295778A>C	NC_000006.12:g.35295778A>G
GRCh37.p13 chr 6	NC_000006.11:g.35263555=	NC_000006.11:g.35263555A>C	NC_000006.11:g.35263555A>G
ZNF76 transcript variant 1	NM_003427.5:c.*530=	NM_003427.5:c.*530A>C	NM_003427.5:c.*530A>G
ZNF76 transcript variant 1	NM_003427.4:c.*530=	NM_003427.4:c.*530A>C	NM_003427.4:c.*530A>G
ZNF76 transcript	NM_003427.3:c.*530G>A	NM_003427.3:c.*530G>C	NM_003427.3:c.*530=
ZNF76 transcript variant X3	XM_017011249.3:c.*530=	XM_017011249.3:c.*530A>C	XM_017011249.3:c.*530A>G
ZNF76 transcript variant X6	XM_017011249.2:c.*530=	XM_017011249.2:c.*530A>C	XM_017011249.2:c.*530A>G
ZNF76 transcript variant X6	XM_017011249.1:c.*530=	XM_017011249.1:c.*530A>C	XM_017011249.1:c.*530A>G
ZNF76 transcript variant X11	XM_017011256.2:c.*530=	XM_017011256.2:c.*530A>C	XM_017011256.2:c.*530A>G
ZNF76 transcript variant X16	XM_017011256.1:c.*530=	XM_017011256.1:c.*530A>C	XM_017011256.1:c.*530A>G
ZNF76 transcript variant 2	NM_001292032.2:c.*530=	NM_001292032.2:c.*530A>C	NM_001292032.2:c.*530A>G
ZNF76 transcript variant 2	NM_001292032.1:c.*530=	NM_001292032.1:c.*530A>C	NM_001292032.1:c.*530A>G
ZNF76 transcript variant X10	XM_017011255.2:c.*530=	XM_017011255.2:c.*530A>C	XM_017011255.2:c.*530A>G
ZNF76 transcript variant X15	XM_017011255.1:c.*530=	XM_017011255.1:c.*530A>C	XM_017011255.1:c.*530A>G
ZNF76 transcript variant X5	XM_047419302.1:c.*530=	XM_047419302.1:c.*530A>C	XM_047419302.1:c.*530A>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#.

112 SubSNP, 20 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	WIAF	ss1219	Sep 19, 2000 (36)
2	CGAP-GAI	ss11199	Sep 19, 2000 (52)
3	LEE	ss1518117	Oct 05, 2000 (87)
4	LEE	ss4410414	May 29, 2002 (106)
5	SC_SNP	ss13098657	Dec 05, 2003 (119)
6	CSHL-HAPMAP	ss17104483	Feb 27, 2004 (120)
7	CSHL-HAPMAP	ss17875476	Feb 27, 2004 (120)
8	SSAHASNP	ss22405349	Apr 05, 2004 (121)
9	PERLEGEN	ss23719852	Sep 20, 2004 (123)
10	ABI	ss44680866	Mar 14, 2006 (126)
11	KRIBB_YJKIM	ss65840835	Nov 29, 2006 (127)
12	ILLUMINA	ss75028692	Dec 07, 2007 (129)
13	SI_EXO	ss76886486	Dec 07, 2007 (129)
14	HGSV	ss85811680	Dec 15, 2007 (130)
15	BCMHGSC_JDW	ss93442484	Mar 24, 2008 (129)
16	HUMANGENOME_JCVI	ss98385398	Feb 05, 2009 (130)
17	BGI	ss104302680	Dec 01, 2009 (131)
18	1000GENOMES	ss109945771	Jan 24, 2009 (130)
19	1000GENOMES	ss114203054	Jan 25, 2009 (130)
20	ILLUMINA-UK	ss116416875	Feb 14, 2009 (130)
21	KRIBB_YJKIM	ss119336951	Dec 01, 2009 (131)
22	ENSEMBL	ss143836799	Dec 01, 2009 (131)
23	ENSEMBL	ss143950313	Dec 01, 2009 (131)
24	GMI	ss156799752	Dec 01, 2009 (131)
25	ILLUMINA	ss160019285	Dec 01, 2009 (131)
26	COMPLETE_GENOMICS	ss162241541	Jul 04, 2010 (132)
27	COMPLETE_GENOMICS	ss163396774	Jul 04, 2010 (132)
28	COMPLETE_GENOMICS	ss166499953	Jul 04, 2010 (132)
29	BUSHMAN	ss201681379	Jul 04, 2010 (132)
30	BCM-HGSC-SUB	ss207754487	Jul 04, 2010 (132)
31	1000GENOMES	ss222331623	Jul 14, 2010 (132)
32	1000GENOMES	ss233427378	Jul 14, 2010 (132)
33	1000GENOMES	ss240492896	Jul 15, 2010 (132)
34	BL	ss254239775	May 09, 2011 (134)
35	GMI	ss278752333	May 04, 2012 (137)
36	GMI	ss285385753	Apr 25, 2013 (138)
37	PJP	ss293836517	May 09, 2011 (134)
38	ILLUMINA	ss480142988	Sep 08, 2015 (146)
39	ILLUMINA	ss483468997	May 04, 2012 (137)
40	ILLUMINA	ss485233146	May 04, 2012 (137)
41	ILLUMINA	ss535678422	Sep 08, 2015 (146)
42	TISHKOFF	ss559135359	Apr 25, 2013 (138)
43	SSMP	ss653071103	Apr 25, 2013 (138)
44	ILLUMINA	ss779069111	Aug 21, 2014 (142)
45	ILLUMINA	ss782177867	Aug 21, 2014 (142)
46	ILLUMINA	ss834532554	Aug 21, 2014 (142)
47	EVA-GONL	ss982811817	Aug 21, 2014 (142)
48	JMKIDD_LAB	ss1073528620	Aug 21, 2014 (142)
49	1000GENOMES	ss1319675361	Aug 21, 2014 (142)
50	DDI	ss1430687127	Apr 01, 2015 (144)
51	EVA_GENOME_DK	ss1581626030	Apr 01, 2015 (144)
52	EVA_DECODE	ss1592345040	Apr 01, 2015 (144)
53	EVA_UK10K_ALSPAC	ss1615334393	Apr 01, 2015 (144)
54	EVA_UK10K_TWINSUK	ss1658328426	Apr 01, 2015 (144)
55	EVA_MGP	ss1711126576	Apr 01, 2015 (144)
56	EVA_SVP	ss1712854753	Apr 01, 2015 (144)
57	HAMMER_LAB	ss1804378536	Sep 08, 2015 (146)
58	WEILL_CORNELL_DGM	ss1926068586	Feb 12, 2016 (147)
59	GENOMED	ss1970370494	Jul 19, 2016 (147)
60	JJLAB	ss2023671599	Sep 14, 2016 (149)
61	ILLUMINA	ss2094957754	Dec 20, 2016 (150)
62	ILLUMINA	ss2095182799	Dec 20, 2016 (150)
63	USC_VALOUEV	ss2151848994	Dec 20, 2016 (150)
64	HUMAN_LONGEVITY	ss2283142337	Dec 20, 2016 (150)
65	SYSTEMSBIOZJU	ss2626324131	Nov 08, 2017 (151)
66	ILLUMINA	ss2634438422	Nov 08, 2017 (151)
67	ILLUMINA	ss2635156215	Nov 08, 2017 (151)
68	GRF	ss2707444925	Nov 08, 2017 (151)
69	GNOMAD	ss2837726593	Nov 08, 2017 (151)
70	SWEGEN	ss2998880863	Nov 08, 2017 (151)
71	BIOINF_KMB_FNS_UNIBA	ss3025627834	Nov 08, 2017 (151)
72	CSHL	ss3346910082	Nov 08, 2017 (151)
73	ILLUMINA	ss3629521318	Oct 12, 2018 (152)
74	ILLUMINA	ss3632355935	Oct 12, 2018 (152)
75	ILLUMINA	ss3636784643	Oct 12, 2018 (152)
76	ILLUMINA	ss3643565555	Oct 12, 2018 (152)
77	OMUKHERJEE_ADBS	ss3646337637	Oct 12, 2018 (152)
78	URBANLAB	ss3648327845	Oct 12, 2018 (152)
79	ILLUMINA	ss3653126710	Oct 12, 2018 (152)
80	EGCUT_WGS	ss3666767978	Jul 13, 2019 (153)
81	EVA_DECODE	ss3716985135	Jul 13, 2019 (153)
82	ACPOP	ss3733404361	Jul 13, 2019 (153)
83	EVA	ss3764878164	Jul 13, 2019 (153)
84	PACBIO	ss3785443963	Jul 13, 2019 (153)
85	PACBIO	ss3790800122	Jul 13, 2019 (153)
86	PACBIO	ss3795678736	Jul 13, 2019 (153)
87	KHV_HUMAN_GENOMES	ss3808030990	Jul 13, 2019 (153)
88	EVA	ss3825697104	Apr 26, 2020 (154)
89	EVA	ss3829865118	Apr 26, 2020 (154)
90	EVA	ss3838409998	Apr 26, 2020 (154)
91	EVA	ss3843854111	Apr 26, 2020 (154)
92	SGDP_PRJ	ss3864347509	Apr 26, 2020 (154)
93	KRGDB	ss3911131782	Apr 26, 2020 (154)
94	FSA-LAB	ss3984335126	Apr 26, 2021 (155)
95	FSA-LAB	ss3984335127	Apr 26, 2021 (155)
96	EVA	ss3986035539	Apr 26, 2021 (155)
97	TOPMED	ss4699165026	Apr 26, 2021 (155)
98	TOMMO_GENOMICS	ss5176999561	Apr 26, 2021 (155)
99	1000G_HIGH_COVERAGE	ss5268045306	Oct 17, 2022 (156)
100	EVA	ss5315148086	Oct 17, 2022 (156)
101	EVA	ss5364898255	Oct 17, 2022 (156)
102	HUGCELL_USP	ss5465757522	Oct 17, 2022 (156)
103	EVA	ss5508450545	Oct 17, 2022 (156)
104	1000G_HIGH_COVERAGE	ss5553748127	Oct 17, 2022 (156)
105	SANFORD_IMAGENETICS	ss5640174214	Oct 17, 2022 (156)
106	TOMMO_GENOMICS	ss5714897324	Oct 17, 2022 (156)
107	YY_MCH	ss5807368596	Oct 17, 2022 (156)
108	EVA	ss5842083632	Oct 17, 2022 (156)
109	EVA	ss5855309500	Oct 17, 2022 (156)
110	EVA	ss5883356297	Oct 17, 2022 (156)
111	EVA	ss5968663491	Oct 17, 2022 (156)
112	EVA	ss5980361831	Oct 17, 2022 (156)
113	1000Genomes	NC_000006.11 - 35263555	Oct 12, 2018 (152)
114	1000Genomes_30x	NC_000006.12 - 35295778	Oct 17, 2022 (156)
115	The Avon Longitudinal Study of Parents and Children	NC_000006.11 - 35263555	Oct 12, 2018 (152)
116	Genetic variation in the Estonian population	NC_000006.11 - 35263555	Oct 12, 2018 (152)
117	The Danish reference pan genome	NC_000006.11 - 35263555	Apr 26, 2020 (154)
118	gnomAD - Genomes	NC_000006.12 - 35295778	Apr 26, 2021 (155)
119	Genome of the Netherlands Release 5	NC_000006.11 - 35263555	Apr 26, 2020 (154)
120	HapMap	NC_000006.12 - 35295778	Apr 26, 2020 (154)
121	KOREAN population from KRGDB	NC_000006.11 - 35263555	Apr 26, 2020 (154)
122	Medical Genome Project healthy controls from Spanish population	NC_000006.11 - 35263555	Apr 26, 2020 (154)
123	Northern Sweden	NC_000006.11 - 35263555	Jul 13, 2019 (153)
124	Qatari	NC_000006.11 - 35263555	Apr 26, 2020 (154)
125	SGDP_PRJ	NC_000006.11 - 35263555	Apr 26, 2020 (154)
126	Siberian	NC_000006.11 - 35263555	Apr 26, 2020 (154)
127	8.3KJPN	NC_000006.11 - 35263555	Apr 26, 2021 (155)
128	14KJPN	NC_000006.12 - 35295778	Oct 17, 2022 (156)
129	TopMed	NC_000006.12 - 35295778	Apr 26, 2021 (155)
130	UK 10K study - Twins	NC_000006.11 - 35263555	Oct 12, 2018 (152)
131	A Vietnamese Genetic Variation Database	NC_000006.11 - 35263555	Jul 13, 2019 (153)
132	ALFA	NC_000006.12 - 35295778	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)
rs1046692	Oct 23, 2000 (87)
rs3186682	Jul 03, 2002 (106)
rs59579515	May 25, 2008 (130)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
18309176, ss3911131782	NC_000006.11:35263554:A:C	NC_000006.12:35295777:A:C	(self)
ss2283142337	NC_000006.12:35295777:A:C	NC_000006.12:35295777:A:C	(self)
ss85811680	NC_000006.9:35371532:A:G	NC_000006.12:35295777:A:G	(self)
ss93442484, ss109945771, ss114203054, ss116416875, ss160019285, ss162241541, ss163396774, ss166499953, ss201681379, ss207754487, ss254239775, ss278752333, ss285385753, ss293836517, ss485233146, ss1592345040, ss1712854753, ss2094957754, ss2635156215, ss3643565555	NC_000006.10:35371532:A:G	NC_000006.12:35295777:A:G	(self)
31447376, 17530599, 12506226, 7790969, 7804981, 18309176, 242336, 6689226, 8110516, 16364489, 4365348, 34968868, 17530599, 3893031, ss222331623, ss233427378, ss240492896, ss480142988, ss483468997, ss535678422, ss559135359, ss653071103, ss779069111, ss782177867, ss834532554, ss982811817, ss1073528620, ss1319675361, ss1430687127, ss1581626030, ss1615334393, ss1658328426, ss1711126576, ss1804378536, ss1926068586, ss1970370494, ss2023671599, ss2095182799, ss2151848994, ss2626324131, ss2634438422, ss2707444925, ss2837726593, ss2998880863, ss3346910082, ss3629521318, ss3632355935, ss3636784643, ss3646337637, ss3653126710, ss3666767978, ss3733404361, ss3764878164, ss3785443963, ss3790800122, ss3795678736, ss3825697104, ss3829865118, ss3838409998, ss3864347509, ss3911131782, ss3984335126, ss3984335127, ss3986035539, ss5176999561, ss5315148086, ss5364898255, ss5508450545, ss5640174214, ss5842083632, ss5968663491, ss5980361831	NC_000006.11:35263554:A:G	NC_000006.12:35295777:A:G	(self)
41274062, 221948628, 3107936, 48734428, 536542584, 6492886626, ss2283142337, ss3025627834, ss3648327845, ss3716985135, ss3808030990, ss3843854111, ss4699165026, ss5268045306, ss5465757522, ss5553748127, ss5714897324, ss5807368596, ss5855309500, ss5883356297	NC_000006.12:35295777:A:G	NC_000006.12:35295777:A:G	(self)
ss13098657, ss17104483, ss17875476, ss22405349	NT_007592.13:26060681:A:G	NC_000006.12:35295777:A:G	(self)
ss76886486	NT_007592.14:26121804:A:G	NC_000006.12:35295777:A:G	(self)
ss1219, ss11199, ss1518117, ss4410414, ss23719852, ss44680866, ss65840835, ss75028692, ss98385398, ss104302680, ss119336951, ss143836799, ss143950313, ss156799752	NT_007592.15:35203554:A:G	NC_000006.12:35295777:A:G	(self)

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

No publications for rs1194

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
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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

rs1194