Name: rs1885296
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.

rs1885296

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr6:2970707 (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 / G>C / G>T
Variation Type: SNV Single Nucleotide Variation
Frequency: G=0.169697 (44917/264690, TOPMED)
G=0.167105 (21497/128644, GnomAD)
G=0.07262 (2051/28242, 14KJPN) (+ 14 more)
G=0.07022 (1175/16732, 8.3KJPN)
G=0.1351 (865/6404, 1000G_30x)
G=0.2171 (1111/5118, ALFA)
G=0.1330 (666/5008, 1000G)
G=0.1603 (709/4424, Estonian)
G=0.1718 (662/3854, ALSPAC)
G=0.1756 (651/3708, TWINSUK)
G=0.0621 (182/2930, KOREAN)
G=0.175 (175/998, GoNL)
G=0.172 (103/600, NorthernSweden)
G=0.111 (61/548, SGDP_PRJ)
G=0.111 (24/216, Qatari)
G=0.04 (2/54, Siberian)
G=0.30 (12/40, GENOME_DK)

Clinical Significance: Reported in ClinVar
Gene : Consequence: SERPINB6 : Intron Variant
Publications: 0 citations
Genomic View: See rs on genome

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=0.169697	C=0.830303
gnomAD - Genomes	Global	Study-wide	128644	G=0.167105	C=0.832895
gnomAD - Genomes	European	Sub	70642	G=0.16753	C=0.83247
gnomAD - Genomes	African	Sub	37348	G=0.18555	C=0.81445
gnomAD - Genomes	American	Sub	12406	G=0.15098	C=0.84902
gnomAD - Genomes	Ashkenazi Jewish	Sub	3284	G=0.1099	C=0.8901
gnomAD - Genomes	East Asian	Sub	3032	G=0.0557	C=0.9443
gnomAD - Genomes	Other	Sub	1932	G=0.1703	C=0.8297
14KJPN	JAPANESE	Study-wide	28242	G=0.07262	C=0.92738
8.3KJPN	JAPANESE	Study-wide	16732	G=0.07022	C=0.92978
1000Genomes_30x	Global	Study-wide	6404	G=0.1351	C=0.8649
1000Genomes_30x	African	Sub	1786	G=0.2161	C=0.7839
1000Genomes_30x	Europe	Sub	1266	G=0.1532	C=0.8468
1000Genomes_30x	South Asian	Sub	1202	G=0.0649	C=0.9351
1000Genomes_30x	East Asian	Sub	1170	G=0.0547	C=0.9453
1000Genomes_30x	American	Sub	980	G=0.146	C=0.854
Allele Frequency Aggregator	Total	Global	5118	G=0.2171	A=0.0000, C=0.7829, T=0.0000
Allele Frequency Aggregator	European	Sub	4730	G=0.1937	A=0.0000, C=0.8063, T=0.0000
Allele Frequency Aggregator	Other	Sub	212	G=0.269	A=0.000, C=0.731, T=0.000
Allele Frequency Aggregator	African	Sub	156	G=0.756	A=0.000, C=0.244, T=0.000
Allele Frequency Aggregator	Latin American 2	Sub	16	G=1.00	A=0.00, C=0.00, T=0.00
Allele Frequency Aggregator	Latin American 1	Sub	4	G=1.0	A=0.0, C=0.0, T=0.0
Allele Frequency Aggregator	South Asian	Sub	0	G=0	A=0, C=0, T=0
Allele Frequency Aggregator	Asian	Sub	0	G=0	A=0, C=0, T=0
1000Genomes	Global	Study-wide	5008	G=0.1330	C=0.8670
1000Genomes	African	Sub	1322	G=0.2148	C=0.7852
1000Genomes	East Asian	Sub	1008	G=0.0565	C=0.9435
1000Genomes	Europe	Sub	1006	G=0.1541	C=0.8459
1000Genomes	South Asian	Sub	978	G=0.067	C=0.933
1000Genomes	American	Sub	694	G=0.150	C=0.850
Genetic variation in the Estonian population	Estonian	Study-wide	4424	G=0.1603	C=0.8397
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	G=0.1718	C=0.8282
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	G=0.1756	C=0.8244
KOREAN population from KRGDB	KOREAN	Study-wide	2930	G=0.0621	A=0.0000, C=0.9379, T=0.0000
Genome of the Netherlands Release 5	Genome of the Netherlands	Study-wide	998	G=0.175	C=0.825
Northern Sweden	ACPOP	Study-wide	600	G=0.172	C=0.828
SGDP_PRJ	Global	Study-wide	548	G=0.111	C=0.889
Qatari	Global	Study-wide	216	G=0.111	C=0.889
Siberian	Global	Study-wide	54	G=0.04	C=0.96
The Danish reference pan genome	Danish	Study-wide	40	G=0.30	C=0.70

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.2970707G>A
GRCh38.p14 chr 6	NC_000006.12:g.2970707G>C
GRCh38.p14 chr 6	NC_000006.12:g.2970707G>T
GRCh37.p13 chr 6	NC_000006.11:g.2970941G>A
GRCh37.p13 chr 6	NC_000006.11:g.2970941G>C
GRCh37.p13 chr 6	NC_000006.11:g.2970941G>T
SERPINB6 RefSeqGene	NG_027692.1:g.6459C>T
SERPINB6 RefSeqGene	NG_027692.1:g.6459C>G
SERPINB6 RefSeqGene	NG_027692.1:g.6459C>A

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.-134+826… NM_001195291.3:c.-134+826C>T	N/A	Intron Variant
SERPINB6 transcript variant 3	NM_001271822.2:c.32+410C>T	N/A	Intron Variant
SERPINB6 transcript variant 4	NM_001271823.2:c.47+51C>T	N/A	Intron Variant
SERPINB6 transcript variant 5	NM_001271824.2:c.-11+784C… NM_001271824.2:c.-11+784C>T	N/A	Intron Variant
SERPINB6 transcript variant 7	NM_001297699.2:c.-11+541C… NM_001297699.2:c.-11+541C>T	N/A	Intron Variant
SERPINB6 transcript variant 8	NM_001297700.2:c.-11+885C… NM_001297700.2:c.-11+885C>T	N/A	Intron Variant
SERPINB6 transcript variant 9	NM_001374515.1:c.-134+784… NM_001374515.1:c.-134+784C>T	N/A	Intron Variant
SERPINB6 transcript variant 11	NM_001374517.1:c.-103+410… NM_001374517.1:c.-103+410C>T	N/A	Intron Variant
SERPINB6 transcript variant 1	NM_004568.6:c.-11+826C>T	N/A	Intron Variant
SERPINB6 transcript variant 10	NM_001374516.1:c.-22=	N/A	5 Prime UTR Variant
SERPINB6 transcript variant 6	NM_001271825.2:c.	N/A	Genic Upstream Transcript Variant
SERPINB6 transcript variant 12	NR_164657.1:n.	N/A	Intron Variant
SERPINB6 transcript variant X2	XM_011514672.2:c.-103+826… XM_011514672.2:c.-103+826C>T	N/A	Intron Variant
SERPINB6 transcript variant X3	XM_047418884.1:c.-103+410… XM_047418884.1:c.-103+410C>T	N/A	Intron Variant
SERPINB6 transcript variant X4	XM_047418885.1:c.-103+784… XM_047418885.1:c.-103+784C>T	N/A	Intron Variant
SERPINB6 transcript variant X5	XM_047418887.1:c.-103+541… XM_047418887.1:c.-103+541C>T	N/A	Intron Variant
SERPINB6 transcript variant X9	XM_047418893.1:c.-103+826… XM_047418893.1:c.-103+826C>T	N/A	Intron Variant
SERPINB6 transcript variant X1	XM_047418883.1:c.-1896=	N/A	5 Prime UTR Variant
SERPINB6 transcript variant X6	XM_047418888.1:c.-114=	N/A	5 Prime UTR Variant
SERPINB6 transcript variant X7	XM_047418889.1:c.-1927=	N/A	5 Prime UTR Variant
SERPINB6 transcript variant X11	XM_047418890.1:c.-1907=	N/A	5 Prime UTR Variant
SERPINB6 transcript variant X10	XM_017010941.2:c.-1896=	N/A	5 Prime UTR Variant
SERPINB6 transcript variant X13	XM_024446465.2:c.-114=	N/A	5 Prime UTR Variant
SERPINB6 transcript variant X12	XM_047418891.1:c.	N/A	Genic Upstream Transcript Variant
SERPINB6 transcript variant X8	XM_047418892.1:c.	N/A	Genic Upstream 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.

Allele: C (allele ID: 1261194 )

ClinVar Accession	Disease Names	Clinical Significance
RCV001679868.1	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	C	T
GRCh38.p14 chr 6	NC_000006.12:g.2970707=	NC_000006.12:g.2970707G>A	NC_000006.12:g.2970707G>C	NC_000006.12:g.2970707G>T
GRCh37.p13 chr 6	NC_000006.11:g.2970941=	NC_000006.11:g.2970941G>A	NC_000006.11:g.2970941G>C	NC_000006.11:g.2970941G>T
SERPINB6 RefSeqGene	NG_027692.1:g.6459=	NG_027692.1:g.6459C>T	NG_027692.1:g.6459C>G	NG_027692.1:g.6459C>A
SERPINB6 transcript variant 10	NM_001374516.1:c.-22=	NM_001374516.1:c.-22C>T	NM_001374516.1:c.-22C>G	NM_001374516.1:c.-22C>A
SERPINB6 transcript variant X10	XM_017010941.2:c.-1896=	XM_017010941.2:c.-1896C>T	XM_017010941.2:c.-1896C>G	XM_017010941.2:c.-1896C>A
SERPINB6 transcript variant X7	XM_017010941.1:c.-1896=	XM_017010941.1:c.-1896C>T	XM_017010941.1:c.-1896C>G	XM_017010941.1:c.-1896C>A
SERPINB6 transcript variant X13	XM_024446465.2:c.-114=	XM_024446465.2:c.-114C>T	XM_024446465.2:c.-114C>G	XM_024446465.2:c.-114C>A
SERPINB6 transcript variant X9	XM_024446465.1:c.-114=	XM_024446465.1:c.-114C>T	XM_024446465.1:c.-114C>G	XM_024446465.1:c.-114C>A
SERPINB6 transcript variant X1	XM_047418883.1:c.-1896=	XM_047418883.1:c.-1896C>T	XM_047418883.1:c.-1896C>G	XM_047418883.1:c.-1896C>A
SERPINB6 transcript variant X7	XM_047418889.1:c.-1927=	XM_047418889.1:c.-1927C>T	XM_047418889.1:c.-1927C>G	XM_047418889.1:c.-1927C>A
SERPINB6 transcript variant X11	XM_047418890.1:c.-1907=	XM_047418890.1:c.-1907C>T	XM_047418890.1:c.-1907C>G	XM_047418890.1:c.-1907C>A
SERPINB6 transcript variant X6	XM_047418888.1:c.-114=	XM_047418888.1:c.-114C>T	XM_047418888.1:c.-114C>G	XM_047418888.1:c.-114C>A
SERPINB6 transcript variant 2	NM_001195291.2:c.-134+826=	NM_001195291.2:c.-134+826C>T	NM_001195291.2:c.-134+826C>G	NM_001195291.2:c.-134+826C>A
SERPINB6 transcript variant 2	NM_001195291.3:c.-134+826=	NM_001195291.3:c.-134+826C>T	NM_001195291.3:c.-134+826C>G	NM_001195291.3:c.-134+826C>A
SERPINB6 transcript variant 3	NM_001271822.1:c.32+410=	NM_001271822.1:c.32+410C>T	NM_001271822.1:c.32+410C>G	NM_001271822.1:c.32+410C>A
SERPINB6 transcript variant 3	NM_001271822.2:c.32+410=	NM_001271822.2:c.32+410C>T	NM_001271822.2:c.32+410C>G	NM_001271822.2:c.32+410C>A
SERPINB6 transcript variant 4	NM_001271823.1:c.47+51=	NM_001271823.1:c.47+51C>T	NM_001271823.1:c.47+51C>G	NM_001271823.1:c.47+51C>A
SERPINB6 transcript variant 4	NM_001271823.2:c.47+51=	NM_001271823.2:c.47+51C>T	NM_001271823.2:c.47+51C>G	NM_001271823.2:c.47+51C>A
SERPINB6 transcript variant 5	NM_001271824.1:c.-11+784=	NM_001271824.1:c.-11+784C>T	NM_001271824.1:c.-11+784C>G	NM_001271824.1:c.-11+784C>A
SERPINB6 transcript variant 5	NM_001271824.2:c.-11+784=	NM_001271824.2:c.-11+784C>T	NM_001271824.2:c.-11+784C>G	NM_001271824.2:c.-11+784C>A
SERPINB6 transcript variant 7	NM_001297699.2:c.-11+541=	NM_001297699.2:c.-11+541C>T	NM_001297699.2:c.-11+541C>G	NM_001297699.2:c.-11+541C>A
SERPINB6 transcript variant 8	NM_001297700.2:c.-11+885=	NM_001297700.2:c.-11+885C>T	NM_001297700.2:c.-11+885C>G	NM_001297700.2:c.-11+885C>A
SERPINB6 transcript variant 9	NM_001374515.1:c.-134+784=	NM_001374515.1:c.-134+784C>T	NM_001374515.1:c.-134+784C>G	NM_001374515.1:c.-134+784C>A
SERPINB6 transcript variant 11	NM_001374517.1:c.-103+410=	NM_001374517.1:c.-103+410C>T	NM_001374517.1:c.-103+410C>G	NM_001374517.1:c.-103+410C>A
SERPINB6 transcript variant 1	NM_004568.5:c.-11+826=	NM_004568.5:c.-11+826C>T	NM_004568.5:c.-11+826C>G	NM_004568.5:c.-11+826C>A
SERPINB6 transcript variant 1	NM_004568.6:c.-11+826=	NM_004568.6:c.-11+826C>T	NM_004568.6:c.-11+826C>G	NM_004568.6:c.-11+826C>A
SERPINB6 transcript variant X2	XM_005249182.1:c.-11+541=	XM_005249182.1:c.-11+541C>T	XM_005249182.1:c.-11+541C>G	XM_005249182.1:c.-11+541C>A
SERPINB6 transcript variant X2	XM_011514672.2:c.-103+826=	XM_011514672.2:c.-103+826C>T	XM_011514672.2:c.-103+826C>G	XM_011514672.2:c.-103+826C>A
SERPINB6 transcript variant X3	XM_047418884.1:c.-103+410=	XM_047418884.1:c.-103+410C>T	XM_047418884.1:c.-103+410C>G	XM_047418884.1:c.-103+410C>A
SERPINB6 transcript variant X4	XM_047418885.1:c.-103+784=	XM_047418885.1:c.-103+784C>T	XM_047418885.1:c.-103+784C>G	XM_047418885.1:c.-103+784C>A
SERPINB6 transcript variant X5	XM_047418887.1:c.-103+541=	XM_047418887.1:c.-103+541C>T	XM_047418887.1:c.-103+541C>G	XM_047418887.1:c.-103+541C>A
SERPINB6 transcript variant X9	XM_047418893.1:c.-103+826=	XM_047418893.1:c.-103+826C>T	XM_047418893.1:c.-103+826C>G	XM_047418893.1:c.-103+826C>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#.

75 SubSNP, 17 Frequency, 1 ClinVar submissions

No	Submitter	Submission ID	Date (Build)
1	TSC-CSHL	ss2764811	Jan 12, 2001 (92)
2	SC_SNP	ss12861349	Dec 05, 2003 (119)
3	SC_SNP	ss15747440	Feb 27, 2004 (120)
4	SSAHASNP	ss22472835	Apr 05, 2004 (121)
5	HGSV	ss80694183	Dec 15, 2007 (130)
6	HGSV	ss86202078	Dec 15, 2007 (130)
7	HUMANGENOME_JCVI	ss98361203	Feb 05, 2009 (130)
8	BGI	ss105975416	Feb 05, 2009 (130)
9	1000GENOMES	ss109700016	Jan 24, 2009 (130)
10	1000GENOMES	ss113804213	Jan 25, 2009 (130)
11	ILLUMINA-UK	ss116272720	Feb 14, 2009 (130)
12	ENSEMBL	ss143072499	Dec 01, 2009 (131)
13	GMI	ss156453709	Dec 01, 2009 (131)
14	COMPLETE_GENOMICS	ss161966303	Jul 04, 2010 (132)
15	COMPLETE_GENOMICS	ss163063260	Jul 04, 2010 (132)
16	COMPLETE_GENOMICS	ss166030706	Jul 04, 2010 (132)
17	BUSHMAN	ss201332631	Jul 04, 2010 (132)
18	BCM-HGSC-SUB	ss207428964	Jul 04, 2010 (132)
19	1000GENOMES	ss222170969	Jul 14, 2010 (132)
20	1000GENOMES	ss233296393	Jul 14, 2010 (132)
21	1000GENOMES	ss240387797	Jul 15, 2010 (132)
22	BL	ss253989603	May 09, 2011 (134)
23	GMI	ss278626801	May 04, 2012 (137)
24	GMI	ss285327225	Apr 25, 2013 (138)
25	PJP	ss293584995	May 09, 2011 (134)
26	TISHKOFF	ss558958306	Apr 25, 2013 (138)
27	SSMP	ss652870179	Apr 25, 2013 (138)
28	EVA-GONL	ss982516098	Aug 21, 2014 (142)
29	JMKIDD_LAB	ss1073329595	Aug 21, 2014 (142)
30	1000GENOMES	ss1318718472	Aug 21, 2014 (142)
31	DDI	ss1430616209	Apr 01, 2015 (144)
32	EVA_GENOME_DK	ss1581504531	Apr 01, 2015 (144)
33	EVA_DECODE	ss1592061699	Apr 01, 2015 (144)
34	EVA_UK10K_ALSPAC	ss1614811673	Apr 01, 2015 (144)
35	EVA_UK10K_TWINSUK	ss1657805706	Apr 01, 2015 (144)
36	HAMMER_LAB	ss1804248918	Sep 08, 2015 (146)
37	WEILL_CORNELL_DGM	ss1925773340	Feb 12, 2016 (147)
38	GENOMED	ss1970294397	Jul 19, 2016 (147)
39	USC_VALOUEV	ss2151663134	Dec 20, 2016 (150)
40	SYSTEMSBIOZJU	ss2626238926	Nov 08, 2017 (151)
41	GRF	ss2707247849	Nov 08, 2017 (151)
42	GNOMAD	ss2835088895	Nov 08, 2017 (151)
43	SWEGEN	ss2998412388	Nov 08, 2017 (151)
44	BIOINF_KMB_FNS_UNIBA	ss3025534078	Nov 08, 2017 (151)
45	CSHL	ss3346804579	Nov 08, 2017 (151)
46	URBANLAB	ss3648253411	Oct 12, 2018 (152)
47	EGCUT_WGS	ss3666335482	Jul 13, 2019 (153)
48	EVA_DECODE	ss3716455200	Jul 13, 2019 (153)
49	EVA_DECODE	ss3716455201	Jul 13, 2019 (153)
50	ACPOP	ss3733145571	Jul 13, 2019 (153)
51	EVA	ss3764532188	Jul 13, 2019 (153)
52	PACBIO	ss3785353846	Jul 13, 2019 (153)
53	PACBIO	ss3790721945	Jul 13, 2019 (153)
54	PACBIO	ss3795599102	Jul 13, 2019 (153)
55	KHV_HUMAN_GENOMES	ss3807693074	Jul 13, 2019 (153)
56	EVA	ss3829696633	Apr 26, 2020 (154)
57	EVA	ss3838322809	Apr 26, 2020 (154)
58	EVA	ss3843762622	Apr 26, 2020 (154)
59	SGDP_PRJ	ss3863783107	Apr 26, 2020 (154)
60	KRGDB	ss3910516648	Apr 26, 2020 (154)
61	TOPMED	ss4691577977	Apr 26, 2021 (155)
62	TOMMO_GENOMICS	ss5175875088	Apr 26, 2021 (155)
63	1000G_HIGH_COVERAGE	ss5267176337	Oct 13, 2022 (156)
64	HUGCELL_USP	ss5464991001	Oct 13, 2022 (156)
65	1000G_HIGH_COVERAGE	ss5552497706	Oct 13, 2022 (156)
66	EVA	ss5623934521	Oct 13, 2022 (156)
67	EVA	ss5624153999	Oct 13, 2022 (156)
68	SANFORD_IMAGENETICS	ss5639638012	Oct 13, 2022 (156)
69	TOMMO_GENOMICS	ss5713459084	Oct 13, 2022 (156)
70	EVA	ss5800126836	Oct 13, 2022 (156)
71	YY_MCH	ss5807095345	Oct 13, 2022 (156)
72	EVA	ss5841703918	Oct 13, 2022 (156)
73	EVA	ss5855173894	Oct 13, 2022 (156)
74	EVA	ss5882396270	Oct 13, 2022 (156)
75	EVA	ss5968131011	Oct 13, 2022 (156)
76	1000Genomes	NC_000006.11 - 2970941	Oct 12, 2018 (152)
77	1000Genomes_30x	NC_000006.12 - 2970707	Oct 13, 2022 (156)
78	The Avon Longitudinal Study of Parents and Children	NC_000006.11 - 2970941	Oct 12, 2018 (152)
79	Genetic variation in the Estonian population	NC_000006.11 - 2970941	Oct 12, 2018 (152)
80	The Danish reference pan genome	NC_000006.11 - 2970941	Apr 26, 2020 (154)
81	gnomAD - Genomes	NC_000006.12 - 2970707	Apr 26, 2021 (155)
82	Genome of the Netherlands Release 5	NC_000006.11 - 2970941	Apr 26, 2020 (154)
83	KOREAN population from KRGDB	NC_000006.11 - 2970941	Apr 26, 2020 (154)
84	Northern Sweden	NC_000006.11 - 2970941	Jul 13, 2019 (153)
85	Qatari	NC_000006.11 - 2970941	Apr 26, 2020 (154)
86	SGDP_PRJ	NC_000006.11 - 2970941	Apr 26, 2020 (154)
87	Siberian	NC_000006.11 - 2970941	Apr 26, 2020 (154)
88	8.3KJPN	NC_000006.11 - 2970941	Apr 26, 2021 (155)
89	14KJPN	NC_000006.12 - 2970707	Oct 13, 2022 (156)
90	TopMed	NC_000006.12 - 2970707	Apr 26, 2021 (155)
91	UK 10K study - Twins	NC_000006.11 - 2970941	Oct 12, 2018 (152)
92	ALFA	NC_000006.12 - 2970707	Apr 26, 2021 (155)
93	ClinVar	RCV001679868.1	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).

Associated ID	History Updated (Build)
rs58673696	May 24, 2008 (130)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
17694042, ss3910516648	NC_000006.11:2970940:G:A	NC_000006.12:2970706:G:A	(self)
14362528297, ss3716455200	NC_000006.12:2970706:G:A	NC_000006.12:2970706:G:A	(self)
ss80694183, ss86202078	NC_000006.9:2915939:G:C	NC_000006.12:2970706:G:C	(self)
ss109700016, ss113804213, ss116272720, ss161966303, ss163063260, ss166030706, ss201332631, ss207428964, ss253989603, ss278626801, ss285327225, ss293584995, ss1592061699	NC_000006.10:2915939:G:C	NC_000006.12:2970706:G:C	(self)
30450915, 16948869, 12073730, 7669470, 7523049, 17694042, 6430436, 7815270, 15800087, 4179488, 33844395, 16948869, ss222170969, ss233296393, ss240387797, ss558958306, ss652870179, ss982516098, ss1073329595, ss1318718472, ss1430616209, ss1581504531, ss1614811673, ss1657805706, ss1804248918, ss1925773340, ss1970294397, ss2151663134, ss2626238926, ss2707247849, ss2835088895, ss2998412388, ss3346804579, ss3666335482, ss3733145571, ss3764532188, ss3785353846, ss3790721945, ss3795599102, ss3829696633, ss3838322809, ss3863783107, ss3910516648, ss5175875088, ss5623934521, ss5624153999, ss5639638012, ss5800126836, ss5841703918, ss5968131011	NC_000006.11:2970940:G:C	NC_000006.12:2970706:G:C	(self)
RCV001679868.1, 40023641, 215322574, 47296188, 528955535, 14362528297, ss3025534078, ss3648253411, ss3716455201, ss3807693074, ss3843762622, ss4691577977, ss5267176337, ss5464991001, ss5552497706, ss5713459084, ss5807095345, ss5855173894, ss5882396270	NC_000006.12:2970706:G:C	NC_000006.12:2970706:G:C	(self)
ss2764811, ss98361203, ss105975416, ss143072499, ss156453709	NT_007592.15:2910940:G:C	NC_000006.12:2970706:G:C	(self)
ss12861349	NT_034880.2:2910939:G:C	NC_000006.12:2970706:G:C	(self)
ss15747440, ss22472835	NT_034880.3:2910939:G:C	NC_000006.12:2970706:G:C	(self)
17694042, ss3910516648	NC_000006.11:2970940:G:T	NC_000006.12:2970706:G:T	(self)
14362528297	NC_000006.12:2970706:G:T	NC_000006.12:2970706:G: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 rs1885296

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

rs1885296