Name: rs7453765
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.

rs7453765

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr6:2959594 (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: G>A
Variation Type: SNV Single Nucleotide Variation
Frequency: A=0.307103 (81287/264690, TOPMED)
A=0.292056 (40899/140038, GnomAD)
A=0.31375 (9683/30862, ALFA) (+ 16 more)
A=0.49926 (14108/28258, 14KJPN)
G=0.49899 (8363/16760, 8.3KJPN)
A=0.3409 (2183/6404, 1000G_30x)
A=0.3464 (1735/5008, 1000G)
A=0.3125 (1400/4480, Estonian)
A=0.3217 (1240/3854, ALSPAC)
A=0.3072 (1139/3708, TWINSUK)
A=0.4969 (1456/2930, KOREAN)
A=0.337 (336/998, GoNL)
A=0.313 (188/600, NorthernSweden)
G=0.355 (122/344, SGDP_PRJ)
A=0.314 (101/322, HapMap)
A=0.199 (43/216, Qatari)
A=0.425 (90/212, Vietnamese)
A=0.23 (9/40, GENOME_DK)
G=0.46 (11/24, Siberian)

Clinical Significance: Reported in ClinVar
Gene : Consequence: SERPINB6 : 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: 20231103111315

Population	Group	Sample Size	Ref Allele	Alt Allele	Ref HMOZ	Alt HMOZ	HTRZ	HWEP
Total	Global	30862	G=0.68625	A=0.31375	0.47424	0.101743	0.424017	2
European	Sub	24734	G=0.67583	A=0.32417	0.457427	0.105765	0.436808	0
African	Sub	3168	G=0.8283	A=0.1717	0.691288	0.034722	0.27399	1
African Others	Sub	124	G=0.911	A=0.089	0.83871	0.016129	0.145161	0
African American	Sub	3044	G=0.8249	A=0.1751	0.685283	0.03548	0.279238	1
Asian	Sub	128	G=0.461	A=0.539	0.1875	0.265625	0.546875	0
East Asian	Sub	100	G=0.50	A=0.50	0.22	0.22	0.56	0
Other Asian	Sub	28	G=0.32	A=0.68	0.071429	0.428571	0.5	0
Latin American 1	Sub	168	G=0.655	A=0.345	0.392857	0.083333	0.52381	1
Latin American 2	Sub	700	G=0.533	A=0.467	0.277143	0.211429	0.511429	0
South Asian	Sub	114	G=0.719	A=0.281	0.508772	0.070175	0.421053	0
Other	Sub	1850	G=0.6568	A=0.3432	0.427027	0.113514	0.459459	0

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	G=0.692897	A=0.307103
gnomAD - Genomes	Global	Study-wide	140038	G=0.707944	A=0.292056
gnomAD - Genomes	European	Sub	75838	G=0.68180	A=0.31820
gnomAD - Genomes	African	Sub	41968	G=0.81162	A=0.18838
gnomAD - Genomes	American	Sub	13642	G=0.61369	A=0.38631
gnomAD - Genomes	Ashkenazi Jewish	Sub	3324	G=0.6239	A=0.3761
gnomAD - Genomes	East Asian	Sub	3122	G=0.4785	A=0.5215
gnomAD - Genomes	Other	Sub	2144	G=0.6674	A=0.3326
Allele Frequency Aggregator	Total	Global	30862	G=0.68625	A=0.31375
Allele Frequency Aggregator	European	Sub	24734	G=0.67583	A=0.32417
Allele Frequency Aggregator	African	Sub	3168	G=0.8283	A=0.1717
Allele Frequency Aggregator	Other	Sub	1850	G=0.6568	A=0.3432
Allele Frequency Aggregator	Latin American 2	Sub	700	G=0.533	A=0.467
Allele Frequency Aggregator	Latin American 1	Sub	168	G=0.655	A=0.345
Allele Frequency Aggregator	Asian	Sub	128	G=0.461	A=0.539
Allele Frequency Aggregator	South Asian	Sub	114	G=0.719	A=0.281
14KJPN	JAPANESE	Study-wide	28258	G=0.50074	A=0.49926
8.3KJPN	JAPANESE	Study-wide	16760	G=0.49899	A=0.50101
1000Genomes_30x	Global	Study-wide	6404	G=0.6591	A=0.3409
1000Genomes_30x	African	Sub	1786	G=0.8471	A=0.1529
1000Genomes_30x	Europe	Sub	1266	G=0.6588	A=0.3412
1000Genomes_30x	South Asian	Sub	1202	G=0.6306	A=0.3694
1000Genomes_30x	East Asian	Sub	1170	G=0.5060	A=0.4940
1000Genomes_30x	American	Sub	980	G=0.535	A=0.465
1000Genomes	Global	Study-wide	5008	G=0.6536	A=0.3464
1000Genomes	African	Sub	1322	G=0.8427	A=0.1573
1000Genomes	East Asian	Sub	1008	G=0.5079	A=0.4921
1000Genomes	Europe	Sub	1006	G=0.6561	A=0.3439
1000Genomes	South Asian	Sub	978	G=0.625	A=0.375
1000Genomes	American	Sub	694	G=0.542	A=0.458
Genetic variation in the Estonian population	Estonian	Study-wide	4480	G=0.6875	A=0.3125
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	G=0.6783	A=0.3217
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	G=0.6928	A=0.3072
KOREAN population from KRGDB	KOREAN	Study-wide	2930	G=0.5031	A=0.4969
Genome of the Netherlands Release 5	Genome of the Netherlands	Study-wide	998	G=0.663	A=0.337
Northern Sweden	ACPOP	Study-wide	600	G=0.687	A=0.313
SGDP_PRJ	Global	Study-wide	344	G=0.355	A=0.645
HapMap	Global	Study-wide	322	G=0.686	A=0.314
HapMap	African	Sub	118	G=0.822	A=0.178
HapMap	American	Sub	116	G=0.698	A=0.302
HapMap	Asian	Sub	88	G=0.49	A=0.51
Qatari	Global	Study-wide	216	G=0.801	A=0.199
A Vietnamese Genetic Variation Database	Global	Study-wide	212	G=0.575	A=0.425
The Danish reference pan genome	Danish	Study-wide	40	G=0.78	A=0.23
Siberian	Global	Study-wide	24	G=0.46	A=0.54

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.2959594G>A
GRCh37.p13 chr 6	NC_000006.11:g.2959828G>A
SERPINB6 RefSeqGene	NG_027692.1:g.17572C>T

Gene: SERPINB6, serpin family B member 6 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
SERPINB6 transcript variant 2	NM_001195291.3:c.3-252C>T	N/A	Intron Variant
SERPINB6 transcript variant 3	NM_001271822.2:c.33-252C>T	N/A	Intron Variant
SERPINB6 transcript variant 4	NM_001271823.2:c.48-252C>T	N/A	Intron Variant
SERPINB6 transcript variant 5	NM_001271824.2:c.-10-252C… NM_001271824.2:c.-10-252C>T	N/A	Intron Variant
SERPINB6 transcript variant 6	NM_001271825.2:c.-10-252C… NM_001271825.2:c.-10-252C>T	N/A	Intron Variant
SERPINB6 transcript variant 7	NM_001297699.2:c.-10-252C… NM_001297699.2:c.-10-252C>T	N/A	Intron Variant
SERPINB6 transcript variant 8	NM_001297700.2:c.-10-252C… NM_001297700.2:c.-10-252C>T	N/A	Intron Variant
SERPINB6 transcript variant 9	NM_001374515.1:c.3-252C>T	N/A	Intron Variant
SERPINB6 transcript variant 10	NM_001374516.1:c.-10-252C… NM_001374516.1:c.-10-252C>T	N/A	Intron Variant
SERPINB6 transcript variant 11	NM_001374517.1:c.34-3924C… NM_001374517.1:c.34-3924C>T	N/A	Intron Variant
SERPINB6 transcript variant 1	NM_004568.6:c.-10-252C>T	N/A	Intron Variant
SERPINB6 transcript variant 12	NR_164657.1:n.	N/A	Intron Variant
SERPINB6 transcript variant X2	XM_011514672.2:c.225-252C… XM_011514672.2:c.225-252C>T	N/A	Intron Variant
SERPINB6 transcript variant X10	XM_017010941.2:c.34-3924C… XM_017010941.2:c.34-3924C>T	N/A	Intron Variant
SERPINB6 transcript variant X13	XM_024446465.2:c.34-3924C… XM_024446465.2:c.34-3924C>T	N/A	Intron Variant
SERPINB6 transcript variant X1	XM_047418883.1:c.225-252C… XM_047418883.1:c.225-252C>T	N/A	Intron Variant
SERPINB6 transcript variant X3	XM_047418884.1:c.225-252C… XM_047418884.1:c.225-252C>T	N/A	Intron Variant
SERPINB6 transcript variant X4	XM_047418885.1:c.225-252C… XM_047418885.1:c.225-252C>T	N/A	Intron Variant
SERPINB6 transcript variant X5	XM_047418887.1:c.225-252C… XM_047418887.1:c.225-252C>T	N/A	Intron Variant
SERPINB6 transcript variant X6	XM_047418888.1:c.225-252C… XM_047418888.1:c.225-252C>T	N/A	Intron Variant
SERPINB6 transcript variant X7	XM_047418889.1:c.3-252C>T	N/A	Intron Variant
SERPINB6 transcript variant X11	XM_047418890.1:c.3-252C>T	N/A	Intron Variant
SERPINB6 transcript variant X12	XM_047418891.1:c.-10-252C… XM_047418891.1:c.-10-252C>T	N/A	Intron Variant
SERPINB6 transcript variant X8	XM_047418892.1:c.-10-252C… XM_047418892.1:c.-10-252C>T	N/A	Intron Variant
SERPINB6 transcript variant X9	XM_047418893.1:c.34-3924C… XM_047418893.1:c.34-3924C>T	N/A	Intron 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.

Allele: A (allele ID: 1227048 )

ClinVar Accession	Disease Names	Clinical Significance
RCV001636121.3	not provided	Benign

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	G=	A
GRCh38.p14 chr 6	NC_000006.12:g.2959594=	NC_000006.12:g.2959594G>A
GRCh37.p13 chr 6	NC_000006.11:g.2959828=	NC_000006.11:g.2959828G>A
SERPINB6 RefSeqGene	NG_027692.1:g.17572=	NG_027692.1:g.17572C>T
SERPINB6 transcript variant 2	NM_001195291.2:c.3-252=	NM_001195291.2:c.3-252C>T
SERPINB6 transcript variant 2	NM_001195291.3:c.3-252=	NM_001195291.3:c.3-252C>T
SERPINB6 transcript variant 3	NM_001271822.1:c.33-252=	NM_001271822.1:c.33-252C>T
SERPINB6 transcript variant 3	NM_001271822.2:c.33-252=	NM_001271822.2:c.33-252C>T
SERPINB6 transcript variant 4	NM_001271823.1:c.48-252=	NM_001271823.1:c.48-252C>T
SERPINB6 transcript variant 4	NM_001271823.2:c.48-252=	NM_001271823.2:c.48-252C>T
SERPINB6 transcript variant 5	NM_001271824.1:c.-10-252=	NM_001271824.1:c.-10-252C>T
SERPINB6 transcript variant 5	NM_001271824.2:c.-10-252=	NM_001271824.2:c.-10-252C>T
SERPINB6 transcript variant 6	NM_001271825.1:c.-10-252=	NM_001271825.1:c.-10-252C>T
SERPINB6 transcript variant 6	NM_001271825.2:c.-10-252=	NM_001271825.2:c.-10-252C>T
SERPINB6 transcript variant 7	NM_001297699.2:c.-10-252=	NM_001297699.2:c.-10-252C>T
SERPINB6 transcript variant 8	NM_001297700.2:c.-10-252=	NM_001297700.2:c.-10-252C>T
SERPINB6 transcript variant 9	NM_001374515.1:c.3-252=	NM_001374515.1:c.3-252C>T
SERPINB6 transcript variant 10	NM_001374516.1:c.-10-252=	NM_001374516.1:c.-10-252C>T
SERPINB6 transcript variant 11	NM_001374517.1:c.34-3924=	NM_001374517.1:c.34-3924C>T
SERPINB6 transcript variant 1	NM_004568.5:c.-10-252=	NM_004568.5:c.-10-252C>T
SERPINB6 transcript variant 1	NM_004568.6:c.-10-252=	NM_004568.6:c.-10-252C>T
SERPINB6 transcript variant X1	XM_005249181.1:c.90-252=	XM_005249181.1:c.90-252C>T
SERPINB6 transcript variant X2	XM_005249182.1:c.-10-252=	XM_005249182.1:c.-10-252C>T
SERPINB6 transcript variant X2	XM_011514672.2:c.225-252=	XM_011514672.2:c.225-252C>T
SERPINB6 transcript variant X10	XM_017010941.2:c.34-3924=	XM_017010941.2:c.34-3924C>T
SERPINB6 transcript variant X13	XM_024446465.2:c.34-3924=	XM_024446465.2:c.34-3924C>T
SERPINB6 transcript variant X1	XM_047418883.1:c.225-252=	XM_047418883.1:c.225-252C>T
SERPINB6 transcript variant X3	XM_047418884.1:c.225-252=	XM_047418884.1:c.225-252C>T
SERPINB6 transcript variant X4	XM_047418885.1:c.225-252=	XM_047418885.1:c.225-252C>T
SERPINB6 transcript variant X5	XM_047418887.1:c.225-252=	XM_047418887.1:c.225-252C>T
SERPINB6 transcript variant X6	XM_047418888.1:c.225-252=	XM_047418888.1:c.225-252C>T
SERPINB6 transcript variant X7	XM_047418889.1:c.3-252=	XM_047418889.1:c.3-252C>T
SERPINB6 transcript variant X11	XM_047418890.1:c.3-252=	XM_047418890.1:c.3-252C>T
SERPINB6 transcript variant X12	XM_047418891.1:c.-10-252=	XM_047418891.1:c.-10-252C>T
SERPINB6 transcript variant X8	XM_047418892.1:c.-10-252=	XM_047418892.1:c.-10-252C>T
SERPINB6 transcript variant X9	XM_047418893.1:c.34-3924=	XM_047418893.1:c.34-3924C>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#.

79 SubSNP, 19 Frequency, 1 ClinVar submissions

No	Submitter	Submission ID	Date (Build)
1	SC_JCM	ss11257413	Jul 11, 2003 (116)
2	SC_SNP	ss13152881	Dec 05, 2003 (119)
3	CSHL-HAPMAP	ss17132573	Feb 27, 2004 (120)
4	CSHL-HAPMAP	ss20284774	Feb 27, 2004 (120)
5	PERLEGEN	ss23984600	Sep 20, 2004 (123)
6	ABI	ss44751237	Mar 14, 2006 (126)
7	SI_EXO	ss71642574	May 16, 2007 (127)
8	BGI	ss105975404	Feb 06, 2009 (130)
9	1000GENOMES	ss109699945	Jan 24, 2009 (130)
10	ILLUMINA-UK	ss116272668	Feb 14, 2009 (130)
11	COMPLETE_GENOMICS	ss161966206	Jul 04, 2010 (132)
12	BUSHMAN	ss201332547	Jul 04, 2010 (132)
13	BCM-HGSC-SUB	ss207800133	Jul 04, 2010 (132)
14	1000GENOMES	ss211773738	Jul 14, 2010 (132)
15	1000GENOMES	ss222170919	Jul 14, 2010 (132)
16	1000GENOMES	ss233296355	Jul 14, 2010 (132)
17	1000GENOMES	ss240387771	Jul 15, 2010 (132)
18	GMI	ss278626775	May 04, 2012 (137)
19	GMI	ss285327213	Apr 25, 2013 (138)
20	PJP	ss293584981	May 09, 2011 (134)
21	ILLUMINA	ss484095686	May 04, 2012 (137)
22	ILLUMINA	ss485224478	May 04, 2012 (137)
23	ILLUMINA	ss536285979	Sep 08, 2015 (146)
24	TISHKOFF	ss558958246	Apr 25, 2013 (138)
25	SSMP	ss652870129	Apr 25, 2013 (138)
26	ILLUMINA	ss780524783	Sep 08, 2015 (146)
27	ILLUMINA	ss782492954	Sep 08, 2015 (146)
28	ILLUMINA	ss836016265	Sep 08, 2015 (146)
29	EVA-GONL	ss982515994	Aug 21, 2014 (142)
30	JMKIDD_LAB	ss1073329531	Aug 21, 2014 (142)
31	1000GENOMES	ss1318718162	Aug 21, 2014 (142)
32	DDI	ss1430616186	Apr 01, 2015 (144)
33	EVA_GENOME_DK	ss1581504497	Apr 01, 2015 (144)
34	EVA_DECODE	ss1592061618	Apr 01, 2015 (144)
35	EVA_UK10K_ALSPAC	ss1614811501	Apr 01, 2015 (144)
36	EVA_UK10K_TWINSUK	ss1657805534	Apr 01, 2015 (144)
37	HAMMER_LAB	ss1804248903	Sep 08, 2015 (146)
38	WEILL_CORNELL_DGM	ss1925773259	Feb 12, 2016 (147)
39	GENOMED	ss1970294376	Jul 19, 2016 (147)
40	JJLAB	ss2023501163	Sep 14, 2016 (149)
41	USC_VALOUEV	ss2151663088	Dec 20, 2016 (150)
42	HUMAN_LONGEVITY	ss2281272265	Dec 20, 2016 (150)
43	SYSTEMSBIOZJU	ss2626238900	Nov 08, 2017 (151)
44	ILLUMINA	ss2634390502	Nov 08, 2017 (151)
45	GRF	ss2707247804	Nov 08, 2017 (151)
46	GNOMAD	ss2835088072	Nov 08, 2017 (151)
47	SWEGEN	ss2998412276	Nov 08, 2017 (151)
48	BIOINF_KMB_FNS_UNIBA	ss3025534053	Nov 08, 2017 (151)
49	CSHL	ss3346804536	Nov 08, 2017 (151)
50	ILLUMINA	ss3629428078	Oct 12, 2018 (152)
51	ILLUMINA	ss3632311139	Oct 12, 2018 (152)
52	ILLUMINA	ss3642469028	Oct 12, 2018 (152)
53	EGCUT_WGS	ss3666335326	Jul 13, 2019 (153)
54	EVA_DECODE	ss3716455063	Jul 13, 2019 (153)
55	ACPOP	ss3733145505	Jul 13, 2019 (153)
56	EVA	ss3764532089	Jul 13, 2019 (153)
57	PACBIO	ss3785353816	Jul 13, 2019 (153)
58	PACBIO	ss3790721921	Jul 13, 2019 (153)
59	PACBIO	ss3795599078	Jul 13, 2019 (153)
60	KHV_HUMAN_GENOMES	ss3807692970	Jul 13, 2019 (153)
61	EVA	ss3825688727	Apr 26, 2020 (154)
62	EVA	ss3829696596	Apr 26, 2020 (154)
63	SGDP_PRJ	ss3863782970	Apr 26, 2020 (154)
64	KRGDB	ss3910516492	Apr 26, 2020 (154)
65	TOPMED	ss4691575462	Apr 26, 2021 (155)
66	TOMMO_GENOMICS	ss5175874765	Apr 26, 2021 (155)
67	1000G_HIGH_COVERAGE	ss5267176091	Oct 13, 2022 (156)
68	EVA	ss5315116326	Oct 13, 2022 (156)
69	EVA	ss5363402862	Oct 13, 2022 (156)
70	HUGCELL_USP	ss5464990775	Oct 13, 2022 (156)
71	EVA	ss5508328783	Oct 13, 2022 (156)
72	1000G_HIGH_COVERAGE	ss5552497319	Oct 13, 2022 (156)
73	SANFORD_IMAGENETICS	ss5639637868	Oct 13, 2022 (156)
74	TOMMO_GENOMICS	ss5713458686	Oct 13, 2022 (156)
75	YY_MCH	ss5807095283	Oct 13, 2022 (156)
76	EVA	ss5841703811	Oct 13, 2022 (156)
77	EVA	ss5855173859	Oct 13, 2022 (156)
78	EVA	ss5882395941	Oct 13, 2022 (156)
79	EVA	ss5968130864	Oct 13, 2022 (156)
80	1000Genomes	NC_000006.11 - 2959828	Oct 12, 2018 (152)
81	1000Genomes_30x	NC_000006.12 - 2959594	Oct 13, 2022 (156)
82	The Avon Longitudinal Study of Parents and Children	NC_000006.11 - 2959828	Oct 12, 2018 (152)
83	Genetic variation in the Estonian population	NC_000006.11 - 2959828	Oct 12, 2018 (152)
84	The Danish reference pan genome	NC_000006.11 - 2959828	Apr 26, 2020 (154)
85	gnomAD - Genomes	NC_000006.12 - 2959594	Apr 26, 2021 (155)
86	Genome of the Netherlands Release 5	NC_000006.11 - 2959828	Apr 26, 2020 (154)
87	HapMap	NC_000006.12 - 2959594	Apr 26, 2020 (154)
88	KOREAN population from KRGDB	NC_000006.11 - 2959828	Apr 26, 2020 (154)
89	Northern Sweden	NC_000006.11 - 2959828	Jul 13, 2019 (153)
90	Qatari	NC_000006.11 - 2959828	Apr 26, 2020 (154)
91	SGDP_PRJ	NC_000006.11 - 2959828	Apr 26, 2020 (154)
92	Siberian	NC_000006.11 - 2959828	Apr 26, 2020 (154)
93	8.3KJPN	NC_000006.11 - 2959828	Apr 26, 2021 (155)
94	14KJPN	NC_000006.12 - 2959594	Oct 13, 2022 (156)
95	TopMed	NC_000006.12 - 2959594	Apr 26, 2021 (155)
96	UK 10K study - Twins	NC_000006.11 - 2959828	Oct 12, 2018 (152)
97	A Vietnamese Genetic Variation Database	NC_000006.11 - 2959828	Jul 13, 2019 (153)
98	ALFA	NC_000006.12 - 2959594	Apr 26, 2021 (155)
99	ClinVar	RCV001636121.3	Oct 13, 2022 (156)

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).

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss109699945, ss116272668, ss161966206, ss201332547, ss207800133, ss211773738, ss278626775, ss285327213, ss293584981, ss485224478, ss1592061618	NC_000006.10:2904826:G:A	NC_000006.12:2959593:G:A	(self)
30450591, 16948677, 12073574, 7669436, 7522945, 17693886, 6430370, 7815189, 15799950, 4179442, 33844072, 16948677, 3753749, ss222170919, ss233296355, ss240387771, ss484095686, ss536285979, ss558958246, ss652870129, ss780524783, ss782492954, ss836016265, ss982515994, ss1073329531, ss1318718162, ss1430616186, ss1581504497, ss1614811501, ss1657805534, ss1804248903, ss1925773259, ss1970294376, ss2023501163, ss2151663088, ss2626238900, ss2634390502, ss2707247804, ss2835088072, ss2998412276, ss3346804536, ss3629428078, ss3632311139, ss3642469028, ss3666335326, ss3733145505, ss3764532089, ss3785353816, ss3790721921, ss3795599078, ss3825688727, ss3829696596, ss3863782970, ss3910516492, ss5175874765, ss5315116326, ss5363402862, ss5508328783, ss5639637868, ss5841703811, ss5968130864	NC_000006.11:2959827:G:A	NC_000006.12:2959593:G:A	(self)
RCV001636121.3, 40023254, 215320534, 3045874, 47295790, 528953020, 11973569516, ss2281272265, ss3025534053, ss3716455063, ss3807692970, ss4691575462, ss5267176091, ss5464990775, ss5552497319, ss5713458686, ss5807095283, ss5855173859, ss5882395941	NC_000006.12:2959593:G:A	NC_000006.12:2959593:G:A	(self)
ss23984600, ss44751237, ss71642574, ss105975404	NT_007592.15:2899827:G:A	NC_000006.12:2959593:G:A	(self)
ss11257413, ss13152881	NT_034880.2:2899826:G:A	NC_000006.12:2959593:G:A	(self)
ss17132573, ss20284774	NT_034880.3:2899826:G:A	NC_000006.12:2959593:G:A	(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 rs7453765

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

rs7453765