Name: rs7763421
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.

rs7763421

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr6:44909576 (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>G / A>T
Variation Type: SNV Single Nucleotide Variation
Frequency: G=0.458582 (121382/264690, TOPMED)
G=0.458243 (64121/139928, GnomAD)
G=0.29662 (8382/28258, 14KJPN) (+ 18 more)
G=0.45342 (9462/20868, ALFA)
G=0.29726 (4982/16760, 8.3KJPN)
G=0.3969 (2542/6404, 1000G_30x)
G=0.3956 (1981/5008, 1000G)
G=0.4984 (2233/4480, Estonian)
A=0.4966 (1914/3854, ALSPAC)
A=0.4898 (1816/3708, TWINSUK)
G=0.3314 (971/2930, KOREAN)
G=0.3286 (602/1832, Korea1K)
G=0.4577 (520/1136, Daghestan)
G=0.495 (494/998, GoNL)
G=0.452 (271/600, NorthernSweden)
A=0.323 (102/316, SGDP_PRJ)
G=0.345 (105/304, HapMap)
A=0.421 (91/216, Qatari)
G=0.229 (49/214, Vietnamese)
A=0.39 (17/44, Siberian)
A=0.38 (15/40, GENOME_DK)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: SUPT3H : Intron 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: 20230706150541

Population	Group	Sample Size	Ref Allele	Alt Allele
Total	Global	20868	A=0.54658	G=0.45342, T=0.00000
European	Sub	13878	A=0.50353	G=0.49647, T=0.00000
African	Sub	5264	A=0.6628	G=0.3372, T=0.0000
African Others	Sub	186	A=0.753	G=0.247, T=0.000
African American	Sub	5078	A=0.6595	G=0.3405, T=0.0000
Asian	Sub	114	A=0.711	G=0.289, T=0.000
East Asian	Sub	88	A=0.72	G=0.28, T=0.00
Other Asian	Sub	26	A=0.69	G=0.31, T=0.00
Latin American 1	Sub	146	A=0.534	G=0.466, T=0.000
Latin American 2	Sub	610	A=0.451	G=0.549, T=0.000
South Asian	Sub	100	A=0.69	G=0.31, T=0.00
Other	Sub	756	A=0.563	G=0.437, T=0.000

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=0.541418	G=0.458582
gnomAD - Genomes	Global	Study-wide	139928	A=0.541757	G=0.458243
gnomAD - Genomes	European	Sub	75814	A=0.50158	G=0.49842
gnomAD - Genomes	African	Sub	41918	A=0.63896	G=0.36104
gnomAD - Genomes	American	Sub	13610	A=0.44570	G=0.55430
gnomAD - Genomes	Ashkenazi Jewish	Sub	3320	A=0.4907	G=0.5093
gnomAD - Genomes	East Asian	Sub	3122	A=0.6999	G=0.3001
gnomAD - Genomes	Other	Sub	2144	A=0.5205	G=0.4795
14KJPN	JAPANESE	Study-wide	28258	A=0.70338	G=0.29662
Allele Frequency Aggregator	Total	Global	20868	A=0.54658	G=0.45342, T=0.00000
Allele Frequency Aggregator	European	Sub	13878	A=0.50353	G=0.49647, T=0.00000
Allele Frequency Aggregator	African	Sub	5264	A=0.6628	G=0.3372, T=0.0000
Allele Frequency Aggregator	Other	Sub	756	A=0.563	G=0.437, T=0.000
Allele Frequency Aggregator	Latin American 2	Sub	610	A=0.451	G=0.549, T=0.000
Allele Frequency Aggregator	Latin American 1	Sub	146	A=0.534	G=0.466, T=0.000
Allele Frequency Aggregator	Asian	Sub	114	A=0.711	G=0.289, T=0.000
Allele Frequency Aggregator	South Asian	Sub	100	A=0.69	G=0.31, T=0.00
8.3KJPN	JAPANESE	Study-wide	16760	A=0.70274	G=0.29726
1000Genomes_30x	Global	Study-wide	6404	A=0.6031	G=0.3969
1000Genomes_30x	African	Sub	1786	A=0.6433	G=0.3567
1000Genomes_30x	Europe	Sub	1266	A=0.4724	G=0.5276
1000Genomes_30x	South Asian	Sub	1202	A=0.6764	G=0.3236
1000Genomes_30x	East Asian	Sub	1170	A=0.7145	G=0.2855
1000Genomes_30x	American	Sub	980	A=0.476	G=0.524
1000Genomes	Global	Study-wide	5008	A=0.6044	G=0.3956
1000Genomes	African	Sub	1322	A=0.6407	G=0.3593
1000Genomes	East Asian	Sub	1008	A=0.7222	G=0.2778
1000Genomes	Europe	Sub	1006	A=0.4602	G=0.5398
1000Genomes	South Asian	Sub	978	A=0.674	G=0.326
1000Genomes	American	Sub	694	A=0.476	G=0.524
Genetic variation in the Estonian population	Estonian	Study-wide	4480	A=0.5016	G=0.4984
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	A=0.4966	G=0.5034
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	A=0.4898	G=0.5102
KOREAN population from KRGDB	KOREAN	Study-wide	2930	A=0.6686	G=0.3314
Korean Genome Project	KOREAN	Study-wide	1832	A=0.6714	G=0.3286
Genome-wide autozygosity in Daghestan	Global	Study-wide	1136	A=0.5423	G=0.4577
Genome-wide autozygosity in Daghestan	Daghestan	Sub	628	A=0.527	G=0.473
Genome-wide autozygosity in Daghestan	Near_East	Sub	144	A=0.569	G=0.431
Genome-wide autozygosity in Daghestan	Central Asia	Sub	122	A=0.533	G=0.467
Genome-wide autozygosity in Daghestan	Europe	Sub	108	A=0.537	G=0.463
Genome-wide autozygosity in Daghestan	South Asian	Sub	98	A=0.67	G=0.33
Genome-wide autozygosity in Daghestan	Caucasus	Sub	36	A=0.39	G=0.61
Genome of the Netherlands Release 5	Genome of the Netherlands	Study-wide	998	A=0.505	G=0.495
Northern Sweden	ACPOP	Study-wide	600	A=0.548	G=0.452
SGDP_PRJ	Global	Study-wide	316	A=0.323	G=0.677
HapMap	Global	Study-wide	304	A=0.655	G=0.345
HapMap	African	Sub	116	A=0.690	G=0.310
HapMap	American	Sub	110	A=0.582	G=0.418
HapMap	Asian	Sub	78	A=0.71	G=0.29
Qatari	Global	Study-wide	216	A=0.421	G=0.579
A Vietnamese Genetic Variation Database	Global	Study-wide	214	A=0.771	G=0.229
Siberian	Global	Study-wide	44	A=0.39	G=0.61
The Danish reference pan genome	Danish	Study-wide	40	A=0.38	G=0.62

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.44909576A>G
GRCh38.p14 chr 6	NC_000006.12:g.44909576A>T
GRCh37.p13 chr 6	NC_000006.11:g.44877313A>G
GRCh37.p13 chr 6	NC_000006.11:g.44877313A>T

Gene: SUPT3H, SPT3 homolog, SAGA and STAGA complex component (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
SUPT3H transcript variant 3	NM_001261823.2:c.456+2307… NM_001261823.2:c.456+23077T>C	N/A	Intron Variant
SUPT3H transcript variant 4	NM_001350324.2:c.23+2425… NM_001350324.2:c.23+2425T>C	N/A	Intron Variant
SUPT3H transcript variant 5	NM_001350325.2:c.906+2307… NM_001350325.2:c.906+23077T>C	N/A	Intron Variant
SUPT3H transcript variant 6	NM_001350326.2:c.849+2307… NM_001350326.2:c.849+23077T>C	N/A	Intron Variant
SUPT3H transcript variant 7	NM_001350327.2:c.654+2307… NM_001350327.2:c.654+23077T>C	N/A	Intron Variant
SUPT3H transcript variant 8	NM_001350329.2:c.912+2307… NM_001350329.2:c.912+23077T>C	N/A	Intron Variant
SUPT3H transcript variant 1	NM_003599.4:c.912+23077T>C	N/A	Intron Variant
SUPT3H transcript variant 2	NM_181356.3:c.945+23077T>C	N/A	Intron Variant
SUPT3H transcript variant 9	NR_146632.2:n.	N/A	Intron Variant
SUPT3H transcript variant 10	NR_146633.1:n.	N/A	Intron Variant
SUPT3H transcript variant 11	NR_146634.2:n.	N/A	Intron Variant
SUPT3H transcript variant 12	NR_146635.2:n.	N/A	Intron Variant
SUPT3H transcript variant X2	XM_011514949.4:c.23+2425… XM_011514949.4:c.23+2425T>C	N/A	Intron Variant
SUPT3H transcript variant X3	XM_011514952.3:c.23+2425… XM_011514952.3:c.23+2425T>C	N/A	Intron Variant
SUPT3H transcript variant X4	XM_011514953.4:c.23+2425… XM_011514953.4:c.23+2425T>C	N/A	Intron Variant
SUPT3H transcript variant X5	XM_011514954.4:c.23+2425… XM_011514954.4:c.23+2425T>C	N/A	Intron Variant
SUPT3H transcript variant X17	XM_017011370.2:c.23+2425… XM_017011370.2:c.23+2425T>C	N/A	Intron Variant
SUPT3H transcript variant X10	XM_017011371.2:c.912+2307… XM_017011371.2:c.912+23077T>C	N/A	Intron Variant
SUPT3H transcript variant X14	XM_017011374.3:c.23+2425… XM_017011374.3:c.23+2425T>C	N/A	Intron Variant
SUPT3H transcript variant X7	XM_024446572.2:c.912+2307… XM_024446572.2:c.912+23077T>C	N/A	Intron Variant
SUPT3H transcript variant X8	XM_047419416.1:c.912+2307… XM_047419416.1:c.912+23077T>C	N/A	Intron Variant
SUPT3H transcript variant X11	XM_047419417.1:c.	N/A	Genic Downstream Transcript Variant
SUPT3H transcript variant X9	XR_007059345.1:n.	N/A	Intron Variant
SUPT3H transcript variant X1	XR_926319.4:n.	N/A	Intron Variant
SUPT3H transcript variant X15	XR_001743692.2:n.	N/A	Genic Downstream Transcript Variant
SUPT3H transcript variant X13	XR_007059346.1:n.	N/A	Genic Downstream Transcript Variant
SUPT3H transcript variant X16	XR_007059347.1:n.	N/A	Genic Downstream Transcript Variant
SUPT3H transcript variant X6	XR_926320.1:n.	N/A	Genic Downstream Transcript Variant
SUPT3H transcript variant X12	XR_926321.1:n.	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=	G	T
GRCh38.p14 chr 6	NC_000006.12:g.44909576=	NC_000006.12:g.44909576A>G	NC_000006.12:g.44909576A>T
GRCh37.p13 chr 6	NC_000006.11:g.44877313=	NC_000006.11:g.44877313A>G	NC_000006.11:g.44877313A>T
SUPT3H transcript variant 3	NM_001261823.1:c.456+23077=	NM_001261823.1:c.456+23077T>C	NM_001261823.1:c.456+23077T>A
SUPT3H transcript variant 3	NM_001261823.2:c.456+23077=	NM_001261823.2:c.456+23077T>C	NM_001261823.2:c.456+23077T>A
SUPT3H transcript variant 4	NM_001350324.2:c.*23+2425=	NM_001350324.2:c.*23+2425T>C	NM_001350324.2:c.*23+2425T>A
SUPT3H transcript variant 5	NM_001350325.2:c.906+23077=	NM_001350325.2:c.906+23077T>C	NM_001350325.2:c.906+23077T>A
SUPT3H transcript variant 6	NM_001350326.2:c.849+23077=	NM_001350326.2:c.849+23077T>C	NM_001350326.2:c.849+23077T>A
SUPT3H transcript variant 7	NM_001350327.2:c.654+23077=	NM_001350327.2:c.654+23077T>C	NM_001350327.2:c.654+23077T>A
SUPT3H transcript variant 8	NM_001350329.2:c.912+23077=	NM_001350329.2:c.912+23077T>C	NM_001350329.2:c.912+23077T>A
SUPT3H transcript variant 1	NM_003599.3:c.912+23077=	NM_003599.3:c.912+23077T>C	NM_003599.3:c.912+23077T>A
SUPT3H transcript variant 1	NM_003599.4:c.912+23077=	NM_003599.4:c.912+23077T>C	NM_003599.4:c.912+23077T>A
SUPT3H transcript variant 2	NM_181356.2:c.945+23077=	NM_181356.2:c.945+23077T>C	NM_181356.2:c.945+23077T>A
SUPT3H transcript variant 2	NM_181356.3:c.945+23077=	NM_181356.3:c.945+23077T>C	NM_181356.3:c.945+23077T>A
SUPT3H transcript variant X1	XM_005249450.1:c.912+23077=	XM_005249450.1:c.912+23077T>C	XM_005249450.1:c.912+23077T>A
SUPT3H transcript variant X2	XM_005249451.1:c.912+23077=	XM_005249451.1:c.912+23077T>C	XM_005249451.1:c.912+23077T>A
SUPT3H transcript variant X3	XM_005249452.1:c.912+23077=	XM_005249452.1:c.912+23077T>C	XM_005249452.1:c.912+23077T>A
SUPT3H transcript variant X2	XM_011514949.4:c.*23+2425=	XM_011514949.4:c.*23+2425T>C	XM_011514949.4:c.*23+2425T>A
SUPT3H transcript variant X3	XM_011514952.3:c.*23+2425=	XM_011514952.3:c.*23+2425T>C	XM_011514952.3:c.*23+2425T>A
SUPT3H transcript variant X4	XM_011514953.4:c.*23+2425=	XM_011514953.4:c.*23+2425T>C	XM_011514953.4:c.*23+2425T>A
SUPT3H transcript variant X5	XM_011514954.4:c.*23+2425=	XM_011514954.4:c.*23+2425T>C	XM_011514954.4:c.*23+2425T>A
SUPT3H transcript variant X17	XM_017011370.2:c.*23+2425=	XM_017011370.2:c.*23+2425T>C	XM_017011370.2:c.*23+2425T>A
SUPT3H transcript variant X10	XM_017011371.2:c.912+23077=	XM_017011371.2:c.912+23077T>C	XM_017011371.2:c.912+23077T>A
SUPT3H transcript variant X14	XM_017011374.3:c.*23+2425=	XM_017011374.3:c.*23+2425T>C	XM_017011374.3:c.*23+2425T>A
SUPT3H transcript variant X7	XM_024446572.2:c.912+23077=	XM_024446572.2:c.912+23077T>C	XM_024446572.2:c.912+23077T>A
SUPT3H transcript variant X8	XM_047419416.1:c.912+23077=	XM_047419416.1:c.912+23077T>C	XM_047419416.1:c.912+23077T>A

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#.

73 SubSNP, 21 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	WI_SSAHASNP	ss11817911	Jul 11, 2003 (116)
2	SC_SNP	ss13102904	Dec 05, 2003 (119)
3	CSHL-HAPMAP	ss19688232	Feb 27, 2004 (120)
4	PERLEGEN	ss24439084	Sep 20, 2004 (123)
5	HGSV	ss84586699	Dec 16, 2007 (130)
6	BCMHGSC_JDW	ss93452233	Mar 24, 2008 (129)
7	HUMANGENOME_JCVI	ss98389718	Feb 06, 2009 (130)
8	BGI	ss105997426	Feb 06, 2009 (130)
9	1000GENOMES	ss110043389	Jan 24, 2009 (130)
10	1000GENOMES	ss114299843	Jan 25, 2009 (130)
11	ENSEMBL	ss143326510	Dec 01, 2009 (131)
12	ENSEMBL	ss143877925	Dec 01, 2009 (131)
13	GMI	ss156876131	Dec 01, 2009 (131)
14	COMPLETE_GENOMICS	ss162306869	Jul 04, 2010 (132)
15	COMPLETE_GENOMICS	ss163462871	Jul 04, 2010 (132)
16	BUSHMAN	ss201765349	Jul 04, 2010 (132)
17	1000GENOMES	ss222368477	Jul 14, 2010 (132)
18	1000GENOMES	ss233454280	Jul 14, 2010 (132)
19	1000GENOMES	ss240515008	Jul 15, 2010 (132)
20	BL	ss254289546	May 09, 2011 (134)
21	GMI	ss278778416	May 04, 2012 (137)
22	GMI	ss285396375	Apr 25, 2013 (138)
23	PJP	ss293849571	May 09, 2011 (134)
24	TISHKOFF	ss559178848	Apr 25, 2013 (138)
25	SSMP	ss653118484	Apr 25, 2013 (138)
26	EVA-GONL	ss982884967	Aug 21, 2014 (142)
27	JMKIDD_LAB	ss1073581044	Aug 21, 2014 (142)
28	1000GENOMES	ss1319951115	Aug 21, 2014 (142)
29	HAMMER_LAB	ss1397455133	Sep 08, 2015 (146)
30	DDI	ss1430708128	Apr 01, 2015 (144)
31	EVA_GENOME_DK	ss1581654548	Apr 01, 2015 (144)
32	EVA_DECODE	ss1592421114	Apr 01, 2015 (144)
33	EVA_UK10K_ALSPAC	ss1615486222	Apr 01, 2015 (144)
34	EVA_UK10K_TWINSUK	ss1658480255	Apr 01, 2015 (144)
35	HAMMER_LAB	ss1804409314	Sep 08, 2015 (146)
36	WEILL_CORNELL_DGM	ss1926141332	Feb 12, 2016 (147)
37	GENOMED	ss1970386503	Jul 19, 2016 (147)
38	JJLAB	ss2023710455	Sep 14, 2016 (149)
39	USC_VALOUEV	ss2151889139	Dec 20, 2016 (150)
40	HUMAN_LONGEVITY	ss2283712726	Dec 20, 2016 (150)
41	GRF	ss2707488154	Nov 08, 2017 (151)
42	GNOMAD	ss2838494132	Nov 08, 2017 (151)
43	SWEGEN	ss2998993406	Nov 08, 2017 (151)
44	BIOINF_KMB_FNS_UNIBA	ss3025646261	Nov 08, 2017 (151)
45	CSHL	ss3346942228	Nov 08, 2017 (151)
46	URBANLAB	ss3648341612	Oct 12, 2018 (152)
47	EGCUT_WGS	ss3666885232	Jul 13, 2019 (153)
48	EVA_DECODE	ss3717124755	Jul 13, 2019 (153)
49	ACPOP	ss3733466234	Jul 13, 2019 (153)
50	EVA	ss3764968529	Jul 13, 2019 (153)
51	PACBIO	ss3785461897	Jul 13, 2019 (153)
52	PACBIO	ss3790814603	Jul 13, 2019 (153)
53	PACBIO	ss3795693259	Jul 13, 2019 (153)
54	KHV_HUMAN_GENOMES	ss3808114892	Jul 13, 2019 (153)
55	EVA	ss3829901268	Apr 26, 2020 (154)
56	EVA	ss3838427092	Apr 26, 2020 (154)
57	EVA	ss3843871551	Apr 26, 2020 (154)
58	SGDP_PRJ	ss3864489514	Apr 26, 2020 (154)
59	KRGDB	ss3911296431	Apr 26, 2020 (154)
60	KOGIC	ss3958949789	Apr 26, 2020 (154)
61	TOPMED	ss4701429226	Apr 26, 2021 (155)
62	TOMMO_GENOMICS	ss5177306742	Apr 26, 2021 (155)
63	1000G_HIGH_COVERAGE	ss5268289462	Oct 17, 2022 (156)
64	HUGCELL_USP	ss5465977729	Oct 17, 2022 (156)
65	EVA	ss5508473344	Oct 17, 2022 (156)
66	1000G_HIGH_COVERAGE	ss5554104326	Oct 17, 2022 (156)
67	SANFORD_IMAGENETICS	ss5640311813	Oct 17, 2022 (156)
68	TOMMO_GENOMICS	ss5715297123	Oct 17, 2022 (156)
69	YY_MCH	ss5807429789	Oct 17, 2022 (156)
70	EVA	ss5842182242	Oct 17, 2022 (156)
71	EVA	ss5855339994	Oct 17, 2022 (156)
72	EVA	ss5883637072	Oct 17, 2022 (156)
73	EVA	ss5968808821	Oct 17, 2022 (156)
74	1000Genomes	NC_000006.11 - 44877313	Oct 12, 2018 (152)
75	1000Genomes_30x	NC_000006.12 - 44909576	Oct 17, 2022 (156)
76	The Avon Longitudinal Study of Parents and Children	NC_000006.11 - 44877313	Oct 12, 2018 (152)
77	Genome-wide autozygosity in Daghestan	NC_000006.10 - 44985291	Apr 26, 2020 (154)
78	Genetic variation in the Estonian population	NC_000006.11 - 44877313	Oct 12, 2018 (152)
79	The Danish reference pan genome	NC_000006.11 - 44877313	Apr 26, 2020 (154)
80	gnomAD - Genomes	NC_000006.12 - 44909576	Apr 26, 2021 (155)
81	Genome of the Netherlands Release 5	NC_000006.11 - 44877313	Apr 26, 2020 (154)
82	HapMap	NC_000006.12 - 44909576	Apr 26, 2020 (154)
83	KOREAN population from KRGDB	NC_000006.11 - 44877313	Apr 26, 2020 (154)
84	Korean Genome Project	NC_000006.12 - 44909576	Apr 26, 2020 (154)
85	Northern Sweden	NC_000006.11 - 44877313	Jul 13, 2019 (153)
86	Qatari	NC_000006.11 - 44877313	Apr 26, 2020 (154)
87	SGDP_PRJ	NC_000006.11 - 44877313	Apr 26, 2020 (154)
88	Siberian	NC_000006.11 - 44877313	Apr 26, 2020 (154)
89	8.3KJPN	NC_000006.11 - 44877313	Apr 26, 2021 (155)
90	14KJPN	NC_000006.12 - 44909576	Oct 17, 2022 (156)
91	TopMed	NC_000006.12 - 44909576	Apr 26, 2021 (155)
92	UK 10K study - Twins	NC_000006.11 - 44877313	Oct 12, 2018 (152)
93	A Vietnamese Genetic Variation Database	NC_000006.11 - 44877313	Jul 13, 2019 (153)
94	ALFA	NC_000006.12 - 44909576	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)
rs17337664	Oct 08, 2004 (123)
rs61186226	May 26, 2008 (130)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss84586699	NC_000006.9:44985290:A:G	NC_000006.12:44909575:A:G	(self)
429762, ss93452233, ss110043389, ss114299843, ss162306869, ss163462871, ss201765349, ss254289546, ss278778416, ss285396375, ss293849571, ss1397455133, ss1592421114	NC_000006.10:44985290:A:G	NC_000006.12:44909575:A:G	(self)
31733480, 17698051, 12623480, 7819487, 7875564, 18473825, 6751099, 8183262, 16506494, 4405493, 35276049, 17698051, 3928170, ss222368477, ss233454280, ss240515008, ss559178848, ss653118484, ss982884967, ss1073581044, ss1319951115, ss1430708128, ss1581654548, ss1615486222, ss1658480255, ss1804409314, ss1926141332, ss1970386503, ss2023710455, ss2151889139, ss2707488154, ss2838494132, ss2998993406, ss3346942228, ss3666885232, ss3733466234, ss3764968529, ss3785461897, ss3790814603, ss3795693259, ss3829901268, ss3838427092, ss3864489514, ss3911296431, ss5177306742, ss5508473344, ss5640311813, ss5842182242, ss5968808821	NC_000006.11:44877312:A:G	NC_000006.12:44909575:A:G	(self)
41630261, 223897137, 3122507, 15327790, 49134227, 538806784, 1508615177, ss2283712726, ss3025646261, ss3648341612, ss3717124755, ss3808114892, ss3843871551, ss3958949789, ss4701429226, ss5268289462, ss5465977729, ss5554104326, ss5715297123, ss5807429789, ss5855339994, ss5883637072	NC_000006.12:44909575:A:G	NC_000006.12:44909575:A:G	(self)
ss11817911, ss13102904, ss19688232	NT_007592.13:35674439:A:G	NC_000006.12:44909575:A:G	(self)
ss24439084, ss98389718, ss105997426, ss143326510, ss143877925, ss156876131	NT_007592.15:44817312:A:G	NC_000006.12:44909575:A:G	(self)
1508615177	NC_000006.12:44909575:A:T	NC_000006.12:44909575:A:T	(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 rs7763421

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.

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dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs7763421