Name: rs913535
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.

rs913535

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr6:3416688 (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>T
Variation Type: SNV Single Nucleotide Variation
Frequency: G=0.473104 (125226/264690, TOPMED)
G=0.468834 (65679/140090, GnomAD)
G=0.44665 (13589/30424, ALFA) (+ 18 more)
T=0.46125 (13034/28258, 14KJPN)
T=0.45853 (7685/16760, 8.3KJPN)
G=0.4585 (2936/6404, 1000G_30x)
G=0.4515 (2261/5008, 1000G)
G=0.4650 (2083/4480, Estonian)
G=0.4258 (1641/3854, ALSPAC)
G=0.4204 (1559/3708, TWINSUK)
T=0.4105 (1202/2928, KOREAN)
T=0.4471 (819/1832, Korea1K)
G=0.422 (421/998, GoNL)
G=0.492 (295/600, NorthernSweden)
G=0.257 (108/420, SGDP_PRJ)
G=0.421 (91/216, Qatari)
G=0.500 (107/214, Vietnamese)
T=0.500 (107/214, Vietnamese)
T=0.36 (18/50, Ancient Sardinia)
G=0.33 (14/42, Siberian)
G=0.45 (18/40, GENOME_DK)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: SLC22A23 : Intron Variant
LOC105374890 : Non Coding Transcript 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	30424	G=0.44665	T=0.55335
European	Sub	24604	G=0.43371	T=0.56629
African	Sub	3144	G=0.5337	T=0.4663
African Others	Sub	124	G=0.645	T=0.355
African American	Sub	3020	G=0.5291	T=0.4709
Asian	Sub	124	G=0.468	T=0.532
East Asian	Sub	98	G=0.46	T=0.54
Other Asian	Sub	26	G=0.50	T=0.50
Latin American 1	Sub	160	G=0.425	T=0.575
Latin American 2	Sub	690	G=0.564	T=0.436
South Asian	Sub	114	G=0.211	T=0.789
Other	Sub	1588	G=0.4414	T=0.5586

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=0.473104	T=0.526896
gnomAD - Genomes	Global	Study-wide	140090	G=0.468834	T=0.531166
gnomAD - Genomes	European	Sub	75882	G=0.43628	T=0.56372
gnomAD - Genomes	African	Sub	41970	G=0.51615	T=0.48385
gnomAD - Genomes	American	Sub	13648	G=0.50608	T=0.49392
gnomAD - Genomes	Ashkenazi Jewish	Sub	3318	G=0.4138	T=0.5862
gnomAD - Genomes	East Asian	Sub	3130	G=0.5163	T=0.4837
gnomAD - Genomes	Other	Sub	2142	G=0.4734	T=0.5266
Allele Frequency Aggregator	Total	Global	30424	G=0.44665	T=0.55335
Allele Frequency Aggregator	European	Sub	24604	G=0.43371	T=0.56629
Allele Frequency Aggregator	African	Sub	3144	G=0.5337	T=0.4663
Allele Frequency Aggregator	Other	Sub	1588	G=0.4414	T=0.5586
Allele Frequency Aggregator	Latin American 2	Sub	690	G=0.564	T=0.436
Allele Frequency Aggregator	Latin American 1	Sub	160	G=0.425	T=0.575
Allele Frequency Aggregator	Asian	Sub	124	G=0.468	T=0.532
Allele Frequency Aggregator	South Asian	Sub	114	G=0.211	T=0.789
14KJPN	JAPANESE	Study-wide	28258	G=0.53875	T=0.46125
8.3KJPN	JAPANESE	Study-wide	16760	G=0.54147	T=0.45853
1000Genomes_30x	Global	Study-wide	6404	G=0.4585	T=0.5415
1000Genomes_30x	African	Sub	1786	G=0.5487	T=0.4513
1000Genomes_30x	Europe	Sub	1266	G=0.4226	T=0.5774
1000Genomes_30x	South Asian	Sub	1202	G=0.2504	T=0.7496
1000Genomes_30x	East Asian	Sub	1170	G=0.5000	T=0.5000
1000Genomes_30x	American	Sub	980	G=0.546	T=0.454
1000Genomes	Global	Study-wide	5008	G=0.4515	T=0.5485
1000Genomes	African	Sub	1322	G=0.5522	T=0.4478
1000Genomes	East Asian	Sub	1008	G=0.4950	T=0.5050
1000Genomes	Europe	Sub	1006	G=0.4264	T=0.5736
1000Genomes	South Asian	Sub	978	G=0.234	T=0.766
1000Genomes	American	Sub	694	G=0.539	T=0.461
Genetic variation in the Estonian population	Estonian	Study-wide	4480	G=0.4650	T=0.5350
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	G=0.4258	T=0.5742
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	G=0.4204	T=0.5796
KOREAN population from KRGDB	KOREAN	Study-wide	2928	G=0.5895	A=0.0000, T=0.4105
Korean Genome Project	KOREAN	Study-wide	1832	G=0.5529	T=0.4471
Genome of the Netherlands Release 5	Genome of the Netherlands	Study-wide	998	G=0.422	T=0.578
Northern Sweden	ACPOP	Study-wide	600	G=0.492	T=0.508
SGDP_PRJ	Global	Study-wide	420	G=0.257	T=0.743
Qatari	Global	Study-wide	216	G=0.421	T=0.579
A Vietnamese Genetic Variation Database	Global	Study-wide	214	G=0.500	T=0.500
Ancient Sardinia genome-wide 1240k capture data generation and analysis	Global	Study-wide	50	G=0.64	T=0.36
Siberian	Global	Study-wide	42	G=0.33	T=0.67
The Danish reference pan genome	Danish	Study-wide	40	G=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 6	NC_000006.12:g.3416688G>A
GRCh38.p14 chr 6	NC_000006.12:g.3416688G>T
GRCh37.p13 chr 6	NC_000006.11:g.3416922G>A
GRCh37.p13 chr 6	NC_000006.11:g.3416922G>T

Gene: SLC22A23, solute carrier family 22 member 23 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
SLC22A23 transcript variant 3	NM_001286455.1:c.-189-833… NM_001286455.1:c.-189-833C>T	N/A	Intron Variant
SLC22A23 transcript variant 4	NM_001286456.2:c.655-833C… NM_001286456.2:c.655-833C>T	N/A	Intron Variant
SLC22A23 transcript variant 6	NM_001382317.1:c.655-833C… NM_001382317.1:c.655-833C>T	N/A	Intron Variant
SLC22A23 transcript variant 9	NM_001382320.1:c.654+3921… NM_001382320.1:c.654+39218C>T	N/A	Intron Variant
SLC22A23 transcript variant 1	NM_015482.2:c.655-833C>T	N/A	Intron Variant
SLC22A23 transcript variant 2	NM_021945.6:c.-189-833C>T	N/A	Intron Variant
SLC22A23 transcript variant 7	NM_001382318.1:c.	N/A	Genic Upstream Transcript Variant
SLC22A23 transcript variant 8	NM_001382319.1:c.	N/A	Genic Upstream Transcript Variant
SLC22A23 transcript variant 10	NM_001382321.1:c.	N/A	Genic Upstream Transcript Variant
SLC22A23 transcript variant 5	NR_104448.1:n.	N/A	Intron Variant
SLC22A23 transcript variant 11	NR_168069.1:n.	N/A	Intron Variant
SLC22A23 transcript variant X1	XM_011514801.3:c.727-833C… XM_011514801.3:c.727-833C>T	N/A	Intron Variant
SLC22A23 transcript variant X5	XM_017011180.2:c.133-833C… XM_017011180.2:c.133-833C>T	N/A	Intron Variant
SLC22A23 transcript variant X3	XM_017011183.2:c.727-833C… XM_017011183.2:c.727-833C>T	N/A	Intron Variant
SLC22A23 transcript variant X4	XM_017011185.3:c.727-833C… XM_017011185.3:c.727-833C>T	N/A	Intron Variant
SLC22A23 transcript variant X11	XM_017011186.2:c.-189-833… XM_017011186.2:c.-189-833C>T	N/A	Intron Variant
SLC22A23 transcript variant X7	XM_017011184.2:c.	N/A	Genic Upstream Transcript Variant
SLC22A23 transcript variant X6	XM_047419241.1:c.	N/A	Genic Upstream Transcript Variant
SLC22A23 transcript variant X8	XM_047419242.1:c.	N/A	Genic Upstream Transcript Variant
SLC22A23 transcript variant X9	XM_047419243.1:c.	N/A	Genic Upstream Transcript Variant
SLC22A23 transcript variant X12	XM_047419244.1:c.	N/A	Genic Downstream Transcript Variant
SLC22A23 transcript variant X2	XR_001743575.2:n.	N/A	Intron Variant
SLC22A23 transcript variant X10	XR_007059328.1:n.	N/A	Intron Variant

Gene: LOC105374890, uncharacterized LOC105374890 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
LOC105374890 transcript	XR_926397.3:n.318G>A	N/A	Non Coding Transcript Variant
LOC105374890 transcript	XR_926397.3:n.318G>T	N/A	Non Coding 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	G=	A	T
GRCh38.p14 chr 6	NC_000006.12:g.3416688=	NC_000006.12:g.3416688G>A	NC_000006.12:g.3416688G>T
GRCh37.p13 chr 6	NC_000006.11:g.3416922=	NC_000006.11:g.3416922G>A	NC_000006.11:g.3416922G>T
LOC105374890 transcript	XR_926397.3:n.318=	XR_926397.3:n.318G>A	XR_926397.3:n.318G>T
LOC105374890 transcript variant X2	XR_926397.2:n.225=	XR_926397.2:n.225G>A	XR_926397.2:n.225G>T
LOC105374890 transcript	XR_926397.1:n.299=	XR_926397.1:n.299G>A	XR_926397.1:n.299G>T
SLC22A23 transcript variant 3	NM_001286455.1:c.-189-833=	NM_001286455.1:c.-189-833C>T	NM_001286455.1:c.-189-833C>A
SLC22A23 transcript variant 4	NM_001286456.2:c.655-833=	NM_001286456.2:c.655-833C>T	NM_001286456.2:c.655-833C>A
SLC22A23 transcript variant 6	NM_001382317.1:c.655-833=	NM_001382317.1:c.655-833C>T	NM_001382317.1:c.655-833C>A
SLC22A23 transcript variant 9	NM_001382320.1:c.654+39218=	NM_001382320.1:c.654+39218C>T	NM_001382320.1:c.654+39218C>A
SLC22A23 transcript variant 1	NM_015482.1:c.655-833=	NM_015482.1:c.655-833C>T	NM_015482.1:c.655-833C>A
SLC22A23 transcript variant 1	NM_015482.2:c.655-833=	NM_015482.2:c.655-833C>T	NM_015482.2:c.655-833C>A
SLC22A23 transcript variant 2	NM_021945.5:c.-189-833=	NM_021945.5:c.-189-833C>T	NM_021945.5:c.-189-833C>A
SLC22A23 transcript variant 2	NM_021945.6:c.-189-833=	NM_021945.6:c.-189-833C>T	NM_021945.6:c.-189-833C>A
SLC22A23 transcript variant X1	XM_005249285.1:c.655-833=	XM_005249285.1:c.655-833C>T	XM_005249285.1:c.655-833C>A
SLC22A23 transcript variant X2	XM_005249286.1:c.-189-833=	XM_005249286.1:c.-189-833C>T	XM_005249286.1:c.-189-833C>A
SLC22A23 transcript variant X1	XM_011514801.3:c.727-833=	XM_011514801.3:c.727-833C>T	XM_011514801.3:c.727-833C>A
SLC22A23 transcript variant X5	XM_017011180.2:c.133-833=	XM_017011180.2:c.133-833C>T	XM_017011180.2:c.133-833C>A
SLC22A23 transcript variant X3	XM_017011183.2:c.727-833=	XM_017011183.2:c.727-833C>T	XM_017011183.2:c.727-833C>A
SLC22A23 transcript variant X4	XM_017011185.3:c.727-833=	XM_017011185.3:c.727-833C>T	XM_017011185.3:c.727-833C>A
SLC22A23 transcript variant X11	XM_017011186.2:c.-189-833=	XM_017011186.2:c.-189-833C>T	XM_017011186.2:c.-189-833C>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#.

86 SubSNP, 20 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	TSC-CSHL	ss1348259	Oct 05, 2000 (86)
2	TSC-CSHL	ss5158454	Oct 08, 2002 (108)
3	SC_JCM	ss5980297	Feb 20, 2003 (111)
4	SC_SNP	ss14777537	Dec 05, 2003 (119)
5	CSHL-HAPMAP	ss17123714	Feb 27, 2004 (120)
6	CSHL-HAPMAP	ss19673385	Feb 27, 2004 (120)
7	SSAHASNP	ss22367398	Apr 05, 2004 (121)
8	ABI	ss44773994	Mar 15, 2006 (126)
9	HGSV	ss78166747	Dec 06, 2007 (129)
10	HGSV	ss82062787	Dec 16, 2007 (130)
11	HUMANGENOME_JCVI	ss98468445	Feb 06, 2009 (130)
12	GMI	ss156457804	Dec 01, 2009 (131)
13	COMPLETE_GENOMICS	ss161969630	Jul 04, 2010 (132)
14	COMPLETE_GENOMICS	ss163068666	Jul 04, 2010 (132)
15	COMPLETE_GENOMICS	ss166037793	Jul 04, 2010 (132)
16	BUSHMAN	ss201339221	Jul 04, 2010 (132)
17	BCM-HGSC-SUB	ss207775000	Jul 04, 2010 (132)
18	1000GENOMES	ss211774602	Jul 14, 2010 (132)
19	1000GENOMES	ss222173424	Jul 14, 2010 (132)
20	1000GENOMES	ss233297988	Jul 14, 2010 (132)
21	1000GENOMES	ss240389108	Jul 15, 2010 (132)
22	BL	ss253993148	May 09, 2011 (134)
23	GMI	ss278628355	May 04, 2012 (137)
24	GMI	ss285327876	Apr 25, 2013 (138)
25	PJP	ss293585962	May 09, 2011 (134)
26	ILLUMINA	ss483503683	May 04, 2012 (137)
27	ILLUMINA	ss485230441	May 04, 2012 (137)
28	ILLUMINA	ss535711621	Sep 08, 2015 (146)
29	TISHKOFF	ss558961561	Apr 25, 2013 (138)
30	SSMP	ss652872801	Apr 25, 2013 (138)
31	ILLUMINA	ss780302093	Sep 08, 2015 (146)
32	ILLUMINA	ss782195235	Sep 08, 2015 (146)
33	ILLUMINA	ss835788838	Sep 08, 2015 (146)
34	EVA-GONL	ss982519987	Aug 21, 2014 (142)
35	JMKIDD_LAB	ss1073332720	Aug 21, 2014 (142)
36	1000GENOMES	ss1318733241	Aug 21, 2014 (142)
37	DDI	ss1430617608	Apr 01, 2015 (144)
38	EVA_GENOME_DK	ss1581506011	Apr 01, 2015 (144)
39	EVA_UK10K_ALSPAC	ss1614819349	Apr 01, 2015 (144)
40	EVA_UK10K_TWINSUK	ss1657813382	Apr 01, 2015 (144)
41	HAMMER_LAB	ss1804251051	Sep 08, 2015 (146)
42	WEILL_CORNELL_DGM	ss1925777784	Feb 12, 2016 (147)
43	GENOMED	ss1970295303	Jul 19, 2016 (147)
44	JJLAB	ss2023503389	Sep 14, 2016 (149)
45	USC_VALOUEV	ss2151665352	Dec 20, 2016 (150)
46	HUMAN_LONGEVITY	ss2281301374	Dec 20, 2016 (150)
47	SYSTEMSBIOZJU	ss2626240103	Nov 08, 2017 (151)
48	ILLUMINA	ss2634391120	Nov 08, 2017 (151)
49	GRF	ss2707250474	Nov 08, 2017 (151)
50	GNOMAD	ss2835129161	Nov 08, 2017 (151)
51	SWEGEN	ss2998418169	Nov 08, 2017 (151)
52	BIOINF_KMB_FNS_UNIBA	ss3025535046	Nov 08, 2017 (151)
53	CSHL	ss3346806573	Nov 08, 2017 (151)
54	ILLUMINA	ss3629429201	Oct 12, 2018 (152)
55	ILLUMINA	ss3632311731	Oct 12, 2018 (152)
56	ILLUMINA	ss3642469305	Oct 12, 2018 (152)
57	URBANLAB	ss3648254485	Oct 12, 2018 (152)
58	EGCUT_WGS	ss3666341771	Jul 13, 2019 (153)
59	EVA_DECODE	ss3716462653	Jul 13, 2019 (153)
60	ACPOP	ss3733148819	Jul 13, 2019 (153)
61	EVA	ss3764536921	Jul 13, 2019 (153)
62	PACBIO	ss3785354884	Jul 13, 2019 (153)
63	PACBIO	ss3790722903	Jul 13, 2019 (153)
64	PACBIO	ss3795600064	Jul 13, 2019 (153)
65	KHV_HUMAN_GENOMES	ss3807698132	Jul 13, 2019 (153)
66	EVA	ss3829698945	Apr 26, 2020 (154)
67	EVA	ss3838323856	Apr 26, 2020 (154)
68	EVA	ss3843763684	Apr 26, 2020 (154)
69	SGDP_PRJ	ss3863791763	Apr 26, 2020 (154)
70	KRGDB	ss3910525584	Apr 26, 2020 (154)
71	KOGIC	ss3958383309	Apr 26, 2020 (154)
72	EVA	ss3985195132	Apr 26, 2021 (155)
73	TOPMED	ss4691691978	Apr 26, 2021 (155)
74	TOMMO_GENOMICS	ss5175892064	Apr 26, 2021 (155)
75	1000G_HIGH_COVERAGE	ss5267189465	Oct 13, 2022 (156)
76	EVA	ss5315116716	Oct 13, 2022 (156)
77	EVA	ss5363426644	Oct 13, 2022 (156)
78	HUGCELL_USP	ss5465002757	Oct 13, 2022 (156)
79	1000G_HIGH_COVERAGE	ss5552516210	Oct 13, 2022 (156)
80	SANFORD_IMAGENETICS	ss5639645818	Oct 13, 2022 (156)
81	TOMMO_GENOMICS	ss5713481580	Oct 13, 2022 (156)
82	YY_MCH	ss5807098667	Oct 13, 2022 (156)
83	EVA	ss5841709311	Oct 13, 2022 (156)
84	EVA	ss5855175731	Oct 13, 2022 (156)
85	EVA	ss5882411193	Oct 13, 2022 (156)
86	EVA	ss5968138837	Oct 13, 2022 (156)
87	1000Genomes	NC_000006.11 - 3416922	Oct 12, 2018 (152)
88	1000Genomes_30x	NC_000006.12 - 3416688	Oct 13, 2022 (156)
89	The Avon Longitudinal Study of Parents and Children	NC_000006.11 - 3416922	Oct 12, 2018 (152)
90	Genetic variation in the Estonian population	NC_000006.11 - 3416922	Oct 12, 2018 (152)
91	The Danish reference pan genome	NC_000006.11 - 3416922	Apr 26, 2020 (154)
92	gnomAD - Genomes	NC_000006.12 - 3416688	Apr 26, 2021 (155)
93	Genome of the Netherlands Release 5	NC_000006.11 - 3416922	Apr 26, 2020 (154)
94	KOREAN population from KRGDB	NC_000006.11 - 3416922	Apr 26, 2020 (154)
95	Korean Genome Project	NC_000006.12 - 3416688	Apr 26, 2020 (154)
96	Northern Sweden	NC_000006.11 - 3416922	Jul 13, 2019 (153)
97	Ancient Sardinia genome-wide 1240k capture data generation and analysis	NC_000006.11 - 3416922	Apr 26, 2021 (155)
98	Qatari	NC_000006.11 - 3416922	Apr 26, 2020 (154)
99	SGDP_PRJ	NC_000006.11 - 3416922	Apr 26, 2020 (154)
100	Siberian	NC_000006.11 - 3416922	Apr 26, 2020 (154)
101	8.3KJPN	NC_000006.11 - 3416922	Apr 26, 2021 (155)
102	14KJPN	NC_000006.12 - 3416688	Oct 13, 2022 (156)
103	TopMed	NC_000006.12 - 3416688	Apr 26, 2021 (155)
104	UK 10K study - Twins	NC_000006.11 - 3416922	Oct 12, 2018 (152)
105	A Vietnamese Genetic Variation Database	NC_000006.11 - 3416922	Jul 13, 2019 (153)
106	ALFA	NC_000006.12 - 3416688	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)
rs61697240	May 27, 2008 (130)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
17702978, ss3910525584	NC_000006.11:3416921:G:A	NC_000006.12:3416687:G:A	(self)
ss78166747, ss82062787	NC_000006.9:3361920:G:T	NC_000006.12:3416687:G:T	(self)
ss161969630, ss163068666, ss166037793, ss201339221, ss207775000, ss211774602, ss253993148, ss278628355, ss285327876, ss293585962, ss485230441	NC_000006.10:3361920:G:T	NC_000006.12:3416687:G:T	(self)
30466278, 16957385, 12080019, 7670950, 7526706, 17702978, 6433684, 421059, 7819714, 15808743, 4181706, 33861371, 16957385, 3755727, ss222173424, ss233297988, ss240389108, ss483503683, ss535711621, ss558961561, ss652872801, ss780302093, ss782195235, ss835788838, ss982519987, ss1073332720, ss1318733241, ss1430617608, ss1581506011, ss1614819349, ss1657813382, ss1804251051, ss1925777784, ss1970295303, ss2023503389, ss2151665352, ss2626240103, ss2634391120, ss2707250474, ss2835129161, ss2998418169, ss3346806573, ss3629429201, ss3632311731, ss3642469305, ss3666341771, ss3733148819, ss3764536921, ss3785354884, ss3790722903, ss3795600064, ss3829698945, ss3838323856, ss3863791763, ss3910525584, ss3985195132, ss5175892064, ss5315116716, ss5363426644, ss5639645818, ss5841709311, ss5968138837	NC_000006.11:3416921:G:T	NC_000006.12:3416687:G:T	(self)
40042145, 215421886, 14761310, 47318684, 529069536, 7783677025, ss2281301374, ss3025535046, ss3648254485, ss3716462653, ss3807698132, ss3843763684, ss3958383309, ss4691691978, ss5267189465, ss5465002757, ss5552516210, ss5713481580, ss5807098667, ss5855175731, ss5882411193	NC_000006.12:3416687:G:T	NC_000006.12:3416687:G:T	(self)
ss1348259, ss5158454, ss5980297, ss44773994, ss98468445, ss156457804	NT_007592.15:3356921:G:T	NC_000006.12:3416687:G:T	(self)
ss14777537, ss17123714, ss19673385, ss22367398	NT_034880.3:3356920:G:T	NC_000006.12:3416687: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 rs913535

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

rs913535