Name: rs10488967
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.

rs10488967

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr4:15983430 (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: C>T
Variation Type: SNV Single Nucleotide Variation
Frequency: T=0.216733 (57367/264690, TOPMED)
T=0.295481 (60596/205076, GENOGRAPHIC)
T=0.226521 (31698/139934, GnomAD) (+ 19 more)
T=0.20214 (5712/28258, 14KJPN)
T=0.26248 (6288/23956, ALFA)
T=0.20155 (3378/16760, 8.3KJPN)
T=0.1747 (1119/6404, 1000G_30x)
T=0.1797 (900/5008, 1000G)
T=0.3051 (1367/4480, Estonian)
T=0.3121 (1203/3854, ALSPAC)
T=0.3066 (1137/3708, TWINSUK)
T=0.1697 (496/2922, KOREAN)
T=0.1497 (283/1890, HapMap)
T=0.299 (298/998, GoNL)
T=0.268 (168/626, Chileans)
T=0.380 (228/600, NorthernSweden)
T=0.241 (52/216, Qatari)
T=0.090 (19/212, Vietnamese)
C=0.419 (88/210, SGDP_PRJ)
T=0.20 (10/50, Ancient Sardinia)
T=0.25 (10/40, GENOME_DK)
C=0.45 (9/20, Siberian)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: PROM1 : 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	23956	C=0.73752	T=0.26248
European	Sub	15666	C=0.69194	T=0.30806
African	Sub	3618	C=0.9362	T=0.0638
African Others	Sub	126	C=0.992	T=0.008
African American	Sub	3492	C=0.9341	T=0.0659
Asian	Sub	160	C=0.887	T=0.113
East Asian	Sub	102	C=0.902	T=0.098
Other Asian	Sub	58	C=0.86	T=0.14
Latin American 1	Sub	290	C=0.790	T=0.210
Latin American 2	Sub	2766	C=0.7155	T=0.2845
South Asian	Sub	110	C=0.727	T=0.273
Other	Sub	1346	C=0.7511	T=0.2489

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	C=0.783267	T=0.216733
Genographic Project	Global	Study-wide	205076	C=0.704519	T=0.295481
gnomAD - Genomes	Global	Study-wide	139934	C=0.773479	T=0.226521
gnomAD - Genomes	European	Sub	75762	C=0.68330	T=0.31670
gnomAD - Genomes	African	Sub	41942	C=0.93763	T=0.06237
gnomAD - Genomes	American	Sub	13630	C=0.76273	T=0.23727
gnomAD - Genomes	Ashkenazi Jewish	Sub	3320	C=0.7108	T=0.2892
gnomAD - Genomes	East Asian	Sub	3130	C=0.8703	T=0.1297
gnomAD - Genomes	Other	Sub	2150	C=0.7730	T=0.2270
14KJPN	JAPANESE	Study-wide	28258	C=0.79786	T=0.20214
Allele Frequency Aggregator	Total	Global	23956	C=0.73752	T=0.26248
Allele Frequency Aggregator	European	Sub	15666	C=0.69194	T=0.30806
Allele Frequency Aggregator	African	Sub	3618	C=0.9362	T=0.0638
Allele Frequency Aggregator	Latin American 2	Sub	2766	C=0.7155	T=0.2845
Allele Frequency Aggregator	Other	Sub	1346	C=0.7511	T=0.2489
Allele Frequency Aggregator	Latin American 1	Sub	290	C=0.790	T=0.210
Allele Frequency Aggregator	Asian	Sub	160	C=0.887	T=0.113
Allele Frequency Aggregator	South Asian	Sub	110	C=0.727	T=0.273
8.3KJPN	JAPANESE	Study-wide	16760	C=0.79845	T=0.20155
1000Genomes_30x	Global	Study-wide	6404	C=0.8253	T=0.1747
1000Genomes_30x	African	Sub	1786	C=0.9854	T=0.0146
1000Genomes_30x	Europe	Sub	1266	C=0.7117	T=0.2883
1000Genomes_30x	South Asian	Sub	1202	C=0.6822	T=0.3178
1000Genomes_30x	East Asian	Sub	1170	C=0.8974	T=0.1026
1000Genomes_30x	American	Sub	980	C=0.769	T=0.231
1000Genomes	Global	Study-wide	5008	C=0.8203	T=0.1797
1000Genomes	African	Sub	1322	C=0.9826	T=0.0174
1000Genomes	East Asian	Sub	1008	C=0.8919	T=0.1081
1000Genomes	Europe	Sub	1006	C=0.7197	T=0.2803
1000Genomes	South Asian	Sub	978	C=0.676	T=0.324
1000Genomes	American	Sub	694	C=0.756	T=0.244
Genetic variation in the Estonian population	Estonian	Study-wide	4480	C=0.6949	T=0.3051
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	C=0.6879	T=0.3121
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	C=0.6934	T=0.3066
KOREAN population from KRGDB	KOREAN	Study-wide	2922	C=0.8303	T=0.1697
HapMap	Global	Study-wide	1890	C=0.8503	T=0.1497
HapMap	American	Sub	768	C=0.754	T=0.246
HapMap	African	Sub	692	C=0.984	T=0.016
HapMap	Asian	Sub	254	C=0.850	T=0.150
HapMap	Europe	Sub	176	C=0.744	T=0.256
Genome of the Netherlands Release 5	Genome of the Netherlands	Study-wide	998	C=0.701	T=0.299
Chileans	Chilean	Study-wide	626	C=0.732	T=0.268
Northern Sweden	ACPOP	Study-wide	600	C=0.620	T=0.380
Qatari	Global	Study-wide	216	C=0.759	T=0.241
A Vietnamese Genetic Variation Database	Global	Study-wide	212	C=0.910	T=0.090
SGDP_PRJ	Global	Study-wide	210	C=0.419	T=0.581
Ancient Sardinia genome-wide 1240k capture data generation and analysis	Global	Study-wide	50	C=0.80	T=0.20
The Danish reference pan genome	Danish	Study-wide	40	C=0.75	T=0.25
Siberian	Global	Study-wide	20	C=0.45	T=0.55

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 4	NC_000004.12:g.15983430C>T
GRCh37.p13 chr 4	NC_000004.11:g.15985053C>T
PROM1 RefSeqGene	NG_011696.2:g.105630G>A

Gene: PROM1, prominin 1 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
PROM1 transcript variant 2	NM_001145847.2:c.2346+833… NM_001145847.2:c.2346+833G>A	N/A	Intron Variant
PROM1 transcript variant 3	NM_001145848.2:c.2346+833… NM_001145848.2:c.2346+833G>A	N/A	Intron Variant
PROM1 transcript variant 7	NM_001145849.2:c.2373+833… NM_001145849.2:c.2373+833G>A	N/A	Intron Variant
PROM1 transcript variant 6	NM_001145850.2:c.2373+833… NM_001145850.2:c.2373+833G>A	N/A	Intron Variant
PROM1 transcript variant 5	NM_001145851.2:c.2346+833… NM_001145851.2:c.2346+833G>A	N/A	Intron Variant
PROM1 transcript variant 4	NM_001145852.2:c.2346+833… NM_001145852.2:c.2346+833G>A	N/A	Intron Variant
PROM1 transcript variant 8	NM_001371406.1:c.2346+833… NM_001371406.1:c.2346+833G>A	N/A	Intron Variant
PROM1 transcript variant 9	NM_001371407.1:c.2346+833… NM_001371407.1:c.2346+833G>A	N/A	Intron Variant
PROM1 transcript variant 10	NM_001371408.1:c.2346+833… NM_001371408.1:c.2346+833G>A	N/A	Intron Variant
PROM1 transcript variant 1	NM_006017.3:c.2373+833G>A	N/A	Intron Variant
PROM1 transcript variant X15	XM_005248195.6:c.2346+833… XM_005248195.6:c.2346+833G>A	N/A	Intron Variant
PROM1 transcript variant X18	XM_005248196.6:c.2346+833… XM_005248196.6:c.2346+833G>A	N/A	Intron Variant
PROM1 transcript variant X20	XM_006713974.4:c.2139+833… XM_006713974.4:c.2139+833G>A	N/A	Intron Variant
PROM1 transcript variant X1	XM_011513893.3:c.2373+833… XM_011513893.3:c.2373+833G>A	N/A	Intron Variant
PROM1 transcript variant X3	XM_011513894.4:c.2373+833… XM_011513894.4:c.2373+833G>A	N/A	Intron Variant
PROM1 transcript variant X4	XM_011513895.3:c.2373+833… XM_011513895.3:c.2373+833G>A	N/A	Intron Variant
PROM1 transcript variant X2	XM_011513897.4:c.2373+833… XM_011513897.4:c.2373+833G>A	N/A	Intron Variant
PROM1 transcript variant X10	XM_011513900.3:c.2373+833… XM_011513900.3:c.2373+833G>A	N/A	Intron Variant
PROM1 transcript variant X13	XM_011513902.3:c.2373+833… XM_011513902.3:c.2373+833G>A	N/A	Intron Variant
PROM1 transcript variant X19	XM_011513903.3:c.2166+833… XM_011513903.3:c.2166+833G>A	N/A	Intron Variant
PROM1 transcript variant X12	XM_017008800.2:c.2373+833… XM_017008800.2:c.2373+833G>A	N/A	Intron Variant
PROM1 transcript variant X5	XM_047416370.1:c.2346+833… XM_047416370.1:c.2346+833G>A	N/A	Intron Variant
PROM1 transcript variant X6	XM_047416372.1:c.2346+833… XM_047416372.1:c.2346+833G>A	N/A	Intron Variant
PROM1 transcript variant X7	XM_047416373.1:c.2346+833… XM_047416373.1:c.2346+833G>A	N/A	Intron Variant
PROM1 transcript variant X8	XM_047416374.1:c.2346+833… XM_047416374.1:c.2346+833G>A	N/A	Intron Variant
PROM1 transcript variant X9	XM_047416375.1:c.2346+833… XM_047416375.1:c.2346+833G>A	N/A	Intron Variant
PROM1 transcript variant X11	XM_047416376.1:c.2373+833… XM_047416376.1:c.2373+833G>A	N/A	Intron Variant
PROM1 transcript variant X14	XM_047416377.1:c.2373+833… XM_047416377.1:c.2373+833G>A	N/A	Intron Variant
PROM1 transcript variant X16	XM_047416378.1:c.2346+833… XM_047416378.1:c.2346+833G>A	N/A	Intron Variant
PROM1 transcript variant X17	XM_047416379.1:c.2346+833… XM_047416379.1:c.2346+833G>A	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.

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	C=	T
GRCh38.p14 chr 4	NC_000004.12:g.15983430=	NC_000004.12:g.15983430C>T
GRCh37.p13 chr 4	NC_000004.11:g.15985053=	NC_000004.11:g.15985053C>T
PROM1 RefSeqGene	NG_011696.2:g.105630=	NG_011696.2:g.105630G>A
PROM1 transcript variant 2	NM_001145847.1:c.2346+833=	NM_001145847.1:c.2346+833G>A
PROM1 transcript variant 2	NM_001145847.2:c.2346+833=	NM_001145847.2:c.2346+833G>A
PROM1 transcript variant 3	NM_001145848.1:c.2346+833=	NM_001145848.1:c.2346+833G>A
PROM1 transcript variant 3	NM_001145848.2:c.2346+833=	NM_001145848.2:c.2346+833G>A
PROM1 transcript variant 7	NM_001145849.1:c.2373+833=	NM_001145849.1:c.2373+833G>A
PROM1 transcript variant 7	NM_001145849.2:c.2373+833=	NM_001145849.2:c.2373+833G>A
PROM1 transcript variant 6	NM_001145850.1:c.2373+833=	NM_001145850.1:c.2373+833G>A
PROM1 transcript variant 6	NM_001145850.2:c.2373+833=	NM_001145850.2:c.2373+833G>A
PROM1 transcript variant 5	NM_001145851.1:c.2346+833=	NM_001145851.1:c.2346+833G>A
PROM1 transcript variant 5	NM_001145851.2:c.2346+833=	NM_001145851.2:c.2346+833G>A
PROM1 transcript variant 4	NM_001145852.1:c.2346+833=	NM_001145852.1:c.2346+833G>A
PROM1 transcript variant 4	NM_001145852.2:c.2346+833=	NM_001145852.2:c.2346+833G>A
PROM1 transcript variant 8	NM_001371406.1:c.2346+833=	NM_001371406.1:c.2346+833G>A
PROM1 transcript variant 9	NM_001371407.1:c.2346+833=	NM_001371407.1:c.2346+833G>A
PROM1 transcript variant 10	NM_001371408.1:c.2346+833=	NM_001371408.1:c.2346+833G>A
PROM1 transcript variant 1	NM_006017.2:c.2373+833=	NM_006017.2:c.2373+833G>A
PROM1 transcript variant 1	NM_006017.3:c.2373+833=	NM_006017.3:c.2373+833G>A
PROM1 transcript variant X1	XM_005248194.1:c.2373+833=	XM_005248194.1:c.2373+833G>A
PROM1 transcript variant X2	XM_005248195.1:c.2346+833=	XM_005248195.1:c.2346+833G>A
PROM1 transcript variant X15	XM_005248195.6:c.2346+833=	XM_005248195.6:c.2346+833G>A
PROM1 transcript variant X3	XM_005248196.1:c.2346+833=	XM_005248196.1:c.2346+833G>A
PROM1 transcript variant X18	XM_005248196.6:c.2346+833=	XM_005248196.6:c.2346+833G>A
PROM1 transcript variant X20	XM_006713974.4:c.2139+833=	XM_006713974.4:c.2139+833G>A
PROM1 transcript variant X1	XM_011513893.3:c.2373+833=	XM_011513893.3:c.2373+833G>A
PROM1 transcript variant X3	XM_011513894.4:c.2373+833=	XM_011513894.4:c.2373+833G>A
PROM1 transcript variant X4	XM_011513895.3:c.2373+833=	XM_011513895.3:c.2373+833G>A
PROM1 transcript variant X2	XM_011513897.4:c.2373+833=	XM_011513897.4:c.2373+833G>A
PROM1 transcript variant X10	XM_011513900.3:c.2373+833=	XM_011513900.3:c.2373+833G>A
PROM1 transcript variant X13	XM_011513902.3:c.2373+833=	XM_011513902.3:c.2373+833G>A
PROM1 transcript variant X19	XM_011513903.3:c.2166+833=	XM_011513903.3:c.2166+833G>A
PROM1 transcript variant X12	XM_017008800.2:c.2373+833=	XM_017008800.2:c.2373+833G>A
PROM1 transcript variant X5	XM_047416370.1:c.2346+833=	XM_047416370.1:c.2346+833G>A
PROM1 transcript variant X6	XM_047416372.1:c.2346+833=	XM_047416372.1:c.2346+833G>A
PROM1 transcript variant X7	XM_047416373.1:c.2346+833=	XM_047416373.1:c.2346+833G>A
PROM1 transcript variant X8	XM_047416374.1:c.2346+833=	XM_047416374.1:c.2346+833G>A
PROM1 transcript variant X9	XM_047416375.1:c.2346+833=	XM_047416375.1:c.2346+833G>A
PROM1 transcript variant X11	XM_047416376.1:c.2373+833=	XM_047416376.1:c.2373+833G>A
PROM1 transcript variant X14	XM_047416377.1:c.2373+833=	XM_047416377.1:c.2373+833G>A
PROM1 transcript variant X16	XM_047416378.1:c.2346+833=	XM_047416378.1:c.2346+833G>A
PROM1 transcript variant X17	XM_047416379.1:c.2346+833=	XM_047416379.1:c.2346+833G>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#.

64 SubSNP, 22 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	PERLEGEN	ss14875591	Dec 05, 2003 (119)
2	PERLEGEN	ss24647538	Sep 20, 2004 (123)
3	ABI	ss44577302	Mar 14, 2006 (126)
4	AFFY	ss65955655	Dec 02, 2006 (127)
5	AFFY	ss76758104	Dec 06, 2007 (129)
6	BCMHGSC_JDW	ss92484984	Mar 24, 2008 (129)
7	HUMANGENOME_JCVI	ss98936676	Feb 04, 2009 (130)
8	KRIBB_YJKIM	ss105008928	Feb 04, 2009 (130)
9	ENSEMBL	ss139464636	Dec 01, 2009 (131)
10	ENSEMBL	ss143266066	Dec 01, 2009 (131)
11	COMPLETE_GENOMICS	ss161929947	Jul 04, 2010 (132)
12	1000GENOMES	ss232276693	Jul 14, 2010 (132)
13	1000GENOMES	ss239593495	Jul 15, 2010 (132)
14	GMI	ss277591044	May 04, 2012 (137)
15	GMI	ss284854167	Apr 25, 2013 (138)
16	PJP	ss293294487	May 09, 2011 (134)
17	TISHKOFF	ss557338211	Apr 25, 2013 (138)
18	SSMP	ss651102855	Apr 25, 2013 (138)
19	EVA-GONL	ss979810487	Aug 21, 2014 (142)
20	JMKIDD_LAB	ss1071307766	Aug 21, 2014 (142)
21	1000GENOMES	ss1308601496	Aug 21, 2014 (142)
22	DDI	ss1429787678	Apr 01, 2015 (144)
23	EVA_GENOME_DK	ss1580433132	Apr 01, 2015 (144)
24	EVA_UK10K_ALSPAC	ss1609497383	Apr 01, 2015 (144)
25	EVA_UK10K_TWINSUK	ss1652491416	Apr 01, 2015 (144)
26	EVA_SVP	ss1712654383	Apr 01, 2015 (144)
27	WEILL_CORNELL_DGM	ss1923048910	Feb 12, 2016 (147)
28	JJLAB	ss2022097652	Sep 14, 2016 (149)
29	USC_VALOUEV	ss2150208090	Dec 20, 2016 (150)
30	HUMAN_LONGEVITY	ss2260744687	Dec 20, 2016 (150)
31	ILLUMINA	ss2634087019	Nov 08, 2017 (151)
32	GRF	ss2705652283	Nov 08, 2017 (151)
33	GNOMAD	ss2806108454	Nov 08, 2017 (151)
34	SWEGEN	ss2994210056	Nov 08, 2017 (151)
35	BIOINF_KMB_FNS_UNIBA	ss3024817971	Nov 08, 2017 (151)
36	CSHL	ss3345565733	Nov 08, 2017 (151)
37	URBANLAB	ss3647662086	Oct 12, 2018 (152)
38	EGCUT_WGS	ss3662117949	Jul 13, 2019 (153)
39	ACPOP	ss3730893645	Jul 13, 2019 (153)
40	EVA	ss3761450910	Jul 13, 2019 (153)
41	PACBIO	ss3784631054	Jul 13, 2019 (153)
42	PACBIO	ss3790100140	Jul 13, 2019 (153)
43	PACBIO	ss3794975194	Jul 13, 2019 (153)
44	KHV_HUMAN_GENOMES	ss3804584523	Jul 13, 2019 (153)
45	EVA	ss3828391842	Apr 26, 2020 (154)
46	EVA	ss3837629502	Apr 26, 2020 (154)
47	EVA	ss3843063686	Apr 26, 2020 (154)
48	SGDP_PRJ	ss3858312954	Apr 26, 2020 (154)
49	KRGDB	ss3904462217	Apr 26, 2020 (154)
50	EVA	ss3985054984	Apr 26, 2021 (155)
51	TOPMED	ss4604271819	Apr 26, 2021 (155)
52	TOMMO_GENOMICS	ss5164391601	Apr 26, 2021 (155)
53	1000G_HIGH_COVERAGE	ss5258194316	Oct 17, 2022 (156)
54	GENOGRAPHIC	ss5314496915	Oct 17, 2022 (156)
55	EVA	ss5347176738	Oct 17, 2022 (156)
56	HUGCELL_USP	ss5457077251	Oct 17, 2022 (156)
57	1000G_HIGH_COVERAGE	ss5538706423	Oct 17, 2022 (156)
58	SANFORD_IMAGENETICS	ss5634436305	Oct 17, 2022 (156)
59	TOMMO_GENOMICS	ss5698093956	Oct 17, 2022 (156)
60	YY_MCH	ss5804795669	Oct 17, 2022 (156)
61	EVA	ss5843610379	Oct 17, 2022 (156)
62	EVA	ss5854097295	Oct 17, 2022 (156)
63	EVA	ss5862314958	Oct 17, 2022 (156)
64	EVA	ss5962814131	Oct 17, 2022 (156)
65	1000Genomes	NC_000004.11 - 15985053	Oct 12, 2018 (152)
66	1000Genomes_30x	NC_000004.12 - 15983430	Oct 17, 2022 (156)
67	The Avon Longitudinal Study of Parents and Children	NC_000004.11 - 15985053	Oct 12, 2018 (152)
68	Chileans	NC_000004.11 - 15985053	Apr 26, 2020 (154)
69	Genetic variation in the Estonian population	NC_000004.11 - 15985053	Oct 12, 2018 (152)
70	Genographic Project	NC_000004.12 - 15983430	Oct 17, 2022 (156)
71	The Danish reference pan genome	NC_000004.11 - 15985053	Apr 26, 2020 (154)
72	gnomAD - Genomes	NC_000004.12 - 15983430	Apr 26, 2021 (155)
73	Genome of the Netherlands Release 5	NC_000004.11 - 15985053	Apr 26, 2020 (154)
74	HapMap	NC_000004.12 - 15983430	Apr 26, 2020 (154)
75	KOREAN population from KRGDB	NC_000004.11 - 15985053	Apr 26, 2020 (154)
76	Northern Sweden	NC_000004.11 - 15985053	Jul 13, 2019 (153)
77	Ancient Sardinia genome-wide 1240k capture data generation and analysis	NC_000004.11 - 15985053	Apr 26, 2021 (155)
78	Qatari	NC_000004.11 - 15985053	Apr 26, 2020 (154)
79	SGDP_PRJ	NC_000004.11 - 15985053	Apr 26, 2020 (154)
80	Siberian	NC_000004.11 - 15985053	Apr 26, 2020 (154)
81	8.3KJPN	NC_000004.11 - 15985053	Apr 26, 2021 (155)
82	14KJPN	NC_000004.12 - 15983430	Oct 17, 2022 (156)
83	TopMed	NC_000004.12 - 15983430	Apr 26, 2021 (155)
84	UK 10K study - Twins	NC_000004.11 - 15985053	Oct 12, 2018 (152)
85	A Vietnamese Genetic Variation Database	NC_000004.11 - 15985053	Jul 13, 2019 (153)
86	ALFA	NC_000004.12 - 15983430	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)
rs17386911	Oct 07, 2004 (123)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss92484984, ss161929947, ss277591044, ss284854167, ss293294487, ss1712654383	NC_000004.10:15594150:C:T	NC_000004.12:15983429:C:T	(self)
19954846, 11112563, 309810, 7856197, 6598071, 4890230, 11639611, 4178510, 280911, 5090840, 10329934, 2724444, 22360908, 11112563, 2428542, ss232276693, ss239593495, ss557338211, ss651102855, ss979810487, ss1071307766, ss1308601496, ss1429787678, ss1580433132, ss1609497383, ss1652491416, ss1923048910, ss2022097652, ss2150208090, ss2634087019, ss2705652283, ss2806108454, ss2994210056, ss3345565733, ss3662117949, ss3730893645, ss3761450910, ss3784631054, ss3790100140, ss3794975194, ss3828391842, ss3837629502, ss3858312954, ss3904462217, ss3985054984, ss5164391601, ss5347176738, ss5634436305, ss5843610379, ss5962814131	NC_000004.11:15985052:C:T	NC_000004.12:15983429:C:T	(self)
26232358, 93499, 141443381, 2564298, 31931060, 441649375, 7320140634, ss2260744687, ss3024817971, ss3647662086, ss3804584523, ss3843063686, ss4604271819, ss5258194316, ss5314496915, ss5457077251, ss5538706423, ss5698093956, ss5804795669, ss5854097295, ss5862314958	NC_000004.12:15983429:C:T	NC_000004.12:15983429:C:T	(self)
ss14875591, ss24647538, ss44577302, ss65955655, ss76758104, ss98936676, ss105008928, ss139464636, ss143266066	NT_006316.16:7166849:C:T	NC_000004.12:15983429:C: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 rs10488967

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

rs10488967