Name: rs995513
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.

rs995513

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr1:79615575 (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>A / C>G / C>T
Variation Type: SNV Single Nucleotide Variation
Frequency: C=0.436605 (115565/264690, TOPMED)
C=0.46187 (32479/70320, ALFA)
C=0.21042 (5946/28258, 14KJPN) (+ 13 more)
C=0.21152 (3545/16760, 8.3KJPN)
C=0.3795 (2430/6404, 1000G_30x)
C=0.3796 (1901/5008, 1000G)
C=0.3625 (1624/4480, Estonian)
C=0.2348 (688/2930, KOREAN)
C=0.2500 (458/1832, Korea1K)
C=0.438 (437/998, GoNL)
C=0.392 (235/600, NorthernSweden)
C=0.218 (107/490, SGDP_PRJ)
C=0.411 (129/314, HapMap)
A=0.407 (88/216, Qatari)
C=0.18 (9/50, Siberian)
C=0.33 (13/40, GENOME_DK)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: None
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	70320	C=0.46187	A=0.53813, G=0.00000, T=0.00000
European	Sub	63894	C=0.45709	A=0.54291, G=0.00000, T=0.00000
African	Sub	2412	C=0.5867	A=0.4133, G=0.0000, T=0.0000
African Others	Sub	90	C=0.53	A=0.47, G=0.00, T=0.00
African American	Sub	2322	C=0.5887	A=0.4113, G=0.0000, T=0.0000
Asian	Sub	52	C=0.35	A=0.65, G=0.00, T=0.00
East Asian	Sub	42	C=0.38	A=0.62, G=0.00, T=0.00
Other Asian	Sub	10	C=0.2	A=0.8, G=0.0, T=0.0
Latin American 1	Sub	362	C=0.544	A=0.456, G=0.000, T=0.000
Latin American 2	Sub	122	C=0.566	A=0.434, G=0.000, T=0.000
South Asian	Sub	72	C=0.54	A=0.46, G=0.00, T=0.00
Other	Sub	3406	C=0.4510	A=0.5490, G=0.0000, T=0.0000

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=0.436605	A=0.563395
Allele Frequency Aggregator	Total	Global	70320	C=0.46187	A=0.53813, G=0.00000, T=0.00000
Allele Frequency Aggregator	European	Sub	63894	C=0.45709	A=0.54291, G=0.00000, T=0.00000
Allele Frequency Aggregator	Other	Sub	3406	C=0.4510	A=0.5490, G=0.0000, T=0.0000
Allele Frequency Aggregator	African	Sub	2412	C=0.5867	A=0.4133, G=0.0000, T=0.0000
Allele Frequency Aggregator	Latin American 1	Sub	362	C=0.544	A=0.456, G=0.000, T=0.000
Allele Frequency Aggregator	Latin American 2	Sub	122	C=0.566	A=0.434, G=0.000, T=0.000
Allele Frequency Aggregator	South Asian	Sub	72	C=0.54	A=0.46, G=0.00, T=0.00
Allele Frequency Aggregator	Asian	Sub	52	C=0.35	A=0.65, G=0.00, T=0.00
14KJPN	JAPANESE	Study-wide	28258	C=0.21042	A=0.78958
8.3KJPN	JAPANESE	Study-wide	16760	C=0.21152	A=0.78848
1000Genomes_30x	Global	Study-wide	6404	C=0.3795	A=0.5995, T=0.0211
1000Genomes_30x	African	Sub	1786	C=0.4597	A=0.4675, T=0.0728
1000Genomes_30x	Europe	Sub	1266	C=0.4937	A=0.5063, T=0.0000
1000Genomes_30x	South Asian	Sub	1202	C=0.3594	A=0.6406, T=0.0000
1000Genomes_30x	East Asian	Sub	1170	C=0.2214	A=0.7786, T=0.0000
1000Genomes_30x	American	Sub	980	C=0.299	A=0.696, T=0.005
1000Genomes	Global	Study-wide	5008	C=0.3796	A=0.5992, T=0.0212
1000Genomes	African	Sub	1322	C=0.4607	A=0.4622, T=0.0772
1000Genomes	East Asian	Sub	1008	C=0.2252	A=0.7748, T=0.0000
1000Genomes	Europe	Sub	1006	C=0.4940	A=0.5060, T=0.0000
1000Genomes	South Asian	Sub	978	C=0.367	A=0.633, T=0.000
1000Genomes	American	Sub	694	C=0.301	A=0.693, T=0.006
Genetic variation in the Estonian population	Estonian	Study-wide	4480	C=0.3625	A=0.6375
KOREAN population from KRGDB	KOREAN	Study-wide	2930	C=0.2348	A=0.7652, G=0.0000, T=0.0000
Korean Genome Project	KOREAN	Study-wide	1832	C=0.2500	A=0.7500
Genome of the Netherlands Release 5	Genome of the Netherlands	Study-wide	998	C=0.438	A=0.562
Northern Sweden	ACPOP	Study-wide	600	C=0.392	A=0.608
SGDP_PRJ	Global	Study-wide	490	C=0.218	A=0.773, T=0.008
HapMap	Global	Study-wide	314	C=0.411	A=0.589
HapMap	American	Sub	120	C=0.467	A=0.533
HapMap	African	Sub	104	C=0.510	A=0.490
HapMap	Asian	Sub	90	C=0.22	A=0.78
Qatari	Global	Study-wide	216	C=0.593	A=0.407
Siberian	Global	Study-wide	50	C=0.18	A=0.82
The Danish reference pan genome	Danish	Study-wide	40	C=0.33	A=0.68

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 1	NC_000001.11:g.79615575C>A
GRCh38.p14 chr 1	NC_000001.11:g.79615575C>G
GRCh38.p14 chr 1	NC_000001.11:g.79615575C>T
GRCh37.p13 chr 1	NC_000001.10:g.80081260C>A
GRCh37.p13 chr 1	NC_000001.10:g.80081260C>G
GRCh37.p13 chr 1	NC_000001.10:g.80081260C>T

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=	A	G	T
GRCh38.p14 chr 1	NC_000001.11:g.79615575=	NC_000001.11:g.79615575C>A	NC_000001.11:g.79615575C>G	NC_000001.11:g.79615575C>T
GRCh37.p13 chr 1	NC_000001.10:g.80081260=	NC_000001.10:g.80081260C>A	NC_000001.10:g.80081260C>G	NC_000001.10:g.80081260C>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#.

101 SubSNP, 23 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	TSC-CSHL	ss1453536	Oct 08, 2002 (108)
2	TSC-CSHL	ss3170309	Jun 15, 2001 (96)
3	SC_JCM	ss5612683	Feb 20, 2003 (111)
4	BCM_SSAHASNP	ss9903742	Jul 11, 2003 (116)
5	SC_SNP	ss13395364	Dec 05, 2003 (119)
6	CSHL-HAPMAP	ss16437207	Feb 27, 2004 (120)
7	CSHL-HAPMAP	ss19135320	Feb 27, 2004 (120)
8	SSAHASNP	ss20557223	Apr 05, 2004 (121)
9	PERLEGEN	ss23162303	Sep 20, 2004 (123)
10	ABI	ss43850306	Mar 15, 2006 (126)
11	AFFY	ss76838318	Dec 06, 2007 (129)
12	BCMHGSC_JDW	ss87566114	Mar 23, 2008 (129)
13	HUMANGENOME_JCVI	ss99221040	Feb 05, 2009 (130)
14	BGI	ss102755854	Dec 01, 2009 (131)
15	1000GENOMES	ss108342594	Jan 23, 2009 (130)
16	ILLUMINA-UK	ss118833796	Feb 14, 2009 (130)
17	ENSEMBL	ss138015833	Dec 01, 2009 (131)
18	ENSEMBL	ss138887075	Dec 01, 2009 (131)
19	GMI	ss155233158	Dec 01, 2009 (131)
20	ILLUMINA	ss161028253	Dec 01, 2009 (131)
21	COMPLETE_GENOMICS	ss163558470	Jul 04, 2010 (132)
22	COMPLETE_GENOMICS	ss164624366	Jul 04, 2010 (132)
23	BUSHMAN	ss198670732	Jul 04, 2010 (132)
24	BCM-HGSC-SUB	ss205154919	Jul 04, 2010 (132)
25	1000GENOMES	ss218477326	Jul 14, 2010 (132)
26	1000GENOMES	ss230601868	Jul 14, 2010 (132)
27	1000GENOMES	ss238281596	Jul 15, 2010 (132)
28	BL	ss253214412	May 09, 2011 (134)
29	GMI	ss275891935	May 04, 2012 (137)
30	GMI	ss284080392	Apr 25, 2013 (138)
31	PJP	ss290545595	May 09, 2011 (134)
32	ILLUMINA	ss482063398	May 04, 2012 (137)
33	ILLUMINA	ss483012804	Sep 08, 2015 (146)
34	SSMP	ss648156900	Apr 25, 2013 (138)
35	ILLUMINA	ss832611870	Sep 08, 2015 (146)
36	EVA-GONL	ss975336770	Aug 21, 2014 (142)
37	JMKIDD_LAB	ss1068021974	Aug 21, 2014 (142)
38	1000GENOMES	ss1291567465	Aug 21, 2014 (142)
39	1000GENOMES	ss1291567466	Aug 21, 2014 (142)
40	DDI	ss1425866941	Apr 01, 2015 (144)
41	EVA_GENOME_DK	ss1574175059	Apr 01, 2015 (144)
42	EVA_DECODE	ss1584710365	Apr 01, 2015 (144)
43	EVA_DECODE	ss1584710366	Apr 01, 2015 (144)
44	EVA_UK10K_ALSPAC	ss1600529599	Apr 01, 2015 (144)
45	EVA_UK10K_ALSPAC	ss1600529600	Apr 01, 2015 (144)
46	EVA_UK10K_TWINSUK	ss1643523632	Apr 01, 2015 (144)
47	EVA_UK10K_TWINSUK	ss1643523633	Apr 01, 2015 (144)
48	EVA_SVP	ss1712346353	Apr 01, 2015 (144)
49	ILLUMINA	ss1751934226	Sep 08, 2015 (146)
50	HAMMER_LAB	ss1794612846	Sep 08, 2015 (146)
51	WEILL_CORNELL_DGM	ss1918541267	Feb 12, 2016 (147)
52	GENOMED	ss1966787574	Jul 19, 2016 (147)
53	JJLAB	ss2019790774	Sep 14, 2016 (149)
54	USC_VALOUEV	ss2147806907	Dec 20, 2016 (150)
55	HUMAN_LONGEVITY	ss2163920228	Dec 20, 2016 (150)
56	SYSTEMSBIOZJU	ss2624406092	Nov 08, 2017 (151)
57	ILLUMINA	ss2632536612	Nov 08, 2017 (151)
58	GRF	ss2697727198	Nov 08, 2017 (151)
59	GNOMAD	ss2757078387	Nov 08, 2017 (151)
60	SWEGEN	ss2987083307	Nov 08, 2017 (151)
61	BIOINF_KMB_FNS_UNIBA	ss3023657418	Nov 08, 2017 (151)
62	CSHL	ss3343531129	Nov 08, 2017 (151)
63	ILLUMINA	ss3632897749	Oct 11, 2018 (152)
64	ILLUMINA	ss3633592560	Oct 11, 2018 (152)
65	ILLUMINA	ss3634332444	Oct 11, 2018 (152)
66	ILLUMINA	ss3635286291	Oct 11, 2018 (152)
67	ILLUMINA	ss3636009418	Oct 11, 2018 (152)
68	ILLUMINA	ss3637036733	Oct 11, 2018 (152)
69	ILLUMINA	ss3640039805	Oct 11, 2018 (152)
70	URBANLAB	ss3646699914	Oct 11, 2018 (152)
71	EGCUT_WGS	ss3655162276	Jul 12, 2019 (153)
72	EVA_DECODE	ss3687100786	Jul 12, 2019 (153)
73	EVA_DECODE	ss3687100787	Jul 12, 2019 (153)
74	ACPOP	ss3727193761	Jul 12, 2019 (153)
75	ILLUMINA	ss3744633417	Jul 12, 2019 (153)
76	EVA	ss3746408251	Jul 12, 2019 (153)
77	ILLUMINA	ss3772134715	Jul 12, 2019 (153)
78	PACBIO	ss3783456414	Jul 12, 2019 (153)
79	PACBIO	ss3789107559	Jul 12, 2019 (153)
80	PACBIO	ss3793980311	Jul 12, 2019 (153)
81	KHV_HUMAN_GENOMES	ss3799414128	Jul 12, 2019 (153)
82	EVA	ss3826257410	Apr 25, 2020 (154)
83	EVA	ss3836517065	Apr 25, 2020 (154)
84	EVA	ss3841924086	Apr 25, 2020 (154)
85	SGDP_PRJ	ss3849195910	Apr 25, 2020 (154)
86	KRGDB	ss3894243483	Apr 25, 2020 (154)
87	KOGIC	ss3944833700	Apr 25, 2020 (154)
88	TOPMED	ss4455801995	Apr 25, 2021 (155)
89	TOMMO_GENOMICS	ss5144699313	Apr 25, 2021 (155)
90	1000G_HIGH_COVERAGE	ss5242851256	Oct 12, 2022 (156)
91	1000G_HIGH_COVERAGE	ss5242851257	Oct 12, 2022 (156)
92	EVA	ss5314627921	Oct 12, 2022 (156)
93	HUGCELL_USP	ss5443857049	Oct 12, 2022 (156)
94	HUGCELL_USP	ss5443857050	Oct 12, 2022 (156)
95	1000G_HIGH_COVERAGE	ss5515442066	Oct 12, 2022 (156)
96	SANFORD_IMAGENETICS	ss5625863390	Oct 12, 2022 (156)
97	TOMMO_GENOMICS	ss5669685409	Oct 12, 2022 (156)
98	YY_MCH	ss5800740759	Oct 12, 2022 (156)
99	EVA	ss5832183817	Oct 12, 2022 (156)
100	EVA	ss5848976768	Oct 12, 2022 (156)
101	EVA	ss5937710444	Oct 12, 2022 (156)
102	1000Genomes	NC_000001.10 - 80081260	Oct 11, 2018 (152)
103	1000Genomes_30x	NC_000001.11 - 79615575	Oct 12, 2022 (156)
104	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 1267293 (NC_000001.10:80081259:C:C 1683/3854, NC_000001.10:80081259:C:A 2171/3854) Row 1267294 (NC_000001.10:80081259:C:C 3854/3854, NC_000001.10:80081259:C:T 0/3854)	-	Oct 11, 2018 (152)
105	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 1267293 (NC_000001.10:80081259:C:C 1683/3854, NC_000001.10:80081259:C:A 2171/3854) Row 1267294 (NC_000001.10:80081259:C:C 3854/3854, NC_000001.10:80081259:C:T 0/3854)	-	Oct 11, 2018 (152)
106	Genetic variation in the Estonian population	NC_000001.10 - 80081260	Oct 11, 2018 (152)
107	The Danish reference pan genome	NC_000001.10 - 80081260	Apr 25, 2020 (154)
108	gnomAD - Genomes Submission ignored due to conflicting rows: Row 16325674 (NC_000001.11:79615574:C:A 76580/139276) Row 16325675 (NC_000001.11:79615574:C:G 6/139344) Row 16325676 (NC_000001.11:79615574:C:T 2791/139336)	-	Apr 25, 2021 (155)
109	gnomAD - Genomes Submission ignored due to conflicting rows: Row 16325674 (NC_000001.11:79615574:C:A 76580/139276) Row 16325675 (NC_000001.11:79615574:C:G 6/139344) Row 16325676 (NC_000001.11:79615574:C:T 2791/139336)	-	Apr 25, 2021 (155)
110	gnomAD - Genomes Submission ignored due to conflicting rows: Row 16325674 (NC_000001.11:79615574:C:A 76580/139276) Row 16325675 (NC_000001.11:79615574:C:G 6/139344) Row 16325676 (NC_000001.11:79615574:C:T 2791/139336)	-	Apr 25, 2021 (155)
111	Genome of the Netherlands Release 5	NC_000001.10 - 80081260	Apr 25, 2020 (154)
112	HapMap	NC_000001.11 - 79615575	Apr 25, 2020 (154)
113	KOREAN population from KRGDB	NC_000001.10 - 80081260	Apr 25, 2020 (154)
114	Korean Genome Project	NC_000001.11 - 79615575	Apr 25, 2020 (154)
115	Northern Sweden	NC_000001.10 - 80081260	Jul 12, 2019 (153)
116	Qatari	NC_000001.10 - 80081260	Apr 25, 2020 (154)
117	SGDP_PRJ	NC_000001.10 - 80081260	Apr 25, 2020 (154)
118	Siberian	NC_000001.10 - 80081260	Apr 25, 2020 (154)
119	8.3KJPN	NC_000001.10 - 80081260	Apr 25, 2021 (155)
120	14KJPN	NC_000001.11 - 79615575	Oct 12, 2022 (156)
121	TopMed	NC_000001.11 - 79615575	Apr 25, 2021 (155)
122	UK 10K study - Twins Submission ignored due to conflicting rows: Row 1267293 (NC_000001.10:80081259:C:C 1590/3708, NC_000001.10:80081259:C:A 2118/3708) Row 1267294 (NC_000001.10:80081259:C:C 3707/3708, NC_000001.10:80081259:C:T 1/3708)	-	Oct 11, 2018 (152)
123	UK 10K study - Twins Submission ignored due to conflicting rows: Row 1267293 (NC_000001.10:80081259:C:C 1590/3708, NC_000001.10:80081259:C:A 2118/3708) Row 1267294 (NC_000001.10:80081259:C:C 3707/3708, NC_000001.10:80081259:C:T 1/3708)	-	Oct 11, 2018 (152)
124	ALFA	NC_000001.11 - 79615575	Apr 25, 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)
rs117550275	Aug 16, 2010 (132)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss76838318, ss87566114, ss108342594, ss118833796, ss164624366, ss198670732, ss205154919, ss253214412, ss275891935, ss284080392, ss290545595, ss1584710365, ss1712346353	NC_000001.9:79853847:C:A	NC_000001.11:79615574:C:A	(self)
2310537, 900524, 1571665, 544310, 1420877, 478626, 583197, 1212890, 323261, 2668620, ss218477326, ss230601868, ss238281596, ss482063398, ss483012804, ss648156900, ss832611870, ss975336770, ss1068021974, ss1291567465, ss1425866941, ss1574175059, ss1600529599, ss1643523632, ss1751934226, ss1794612846, ss1918541267, ss1966787574, ss2019790774, ss2147806907, ss2624406092, ss2632536612, ss2697727198, ss2757078387, ss2987083307, ss3343531129, ss3632897749, ss3633592560, ss3634332444, ss3635286291, ss3636009418, ss3637036733, ss3640039805, ss3655162276, ss3727193761, ss3744633417, ss3746408251, ss3772134715, ss3783456414, ss3789107559, ss3793980311, ss3826257410, ss3836517065, ss3849195910, ss3894243483, ss5144699313, ss5314627921, ss5625863390, ss5832183817, ss5937710444	NC_000001.10:80081259:C:A	NC_000001.11:79615574:C:A	(self)
2968001, 106663, 1211701, 3522513, 19408330, 10328933832, ss2163920228, ss3023657418, ss3646699914, ss3687100786, ss3799414128, ss3841924086, ss3944833700, ss4455801995, ss5242851256, ss5443857049, ss5515442066, ss5669685409, ss5800740759, ss5848976768	NC_000001.11:79615574:C:A	NC_000001.11:79615574:C:A	(self)
ss9903742	NT_004483.15:1750330:C:A	NC_000001.11:79615574:C:A	(self)
ss16437207, ss19135320, ss20557223	NT_026943.13:4901433:C:A	NC_000001.11:79615574:C:A	(self)
ss1453536, ss3170309, ss5612683, ss13395364, ss23162303, ss43850306, ss99221040, ss102755854, ss138015833, ss138887075, ss155233158, ss161028253	NT_032977.9:50053177:C:A	NC_000001.11:79615574:C:A	(self)
1420877, ss2757078387, ss3894243483	NC_000001.10:80081259:C:G	NC_000001.11:79615574:C:G	(self)
10328933832	NC_000001.11:79615574:C:G	NC_000001.11:79615574:C:G	(self)
ss163558470, ss1584710366	NC_000001.9:79853847:C:T	NC_000001.11:79615574:C:T	(self)
2310537, 1420877, 1212890, ss1291567466, ss1600529600, ss1643523633, ss2757078387, ss3849195910, ss3894243483, ss5625863390	NC_000001.10:80081259:C:T	NC_000001.11:79615574:C:T	(self)
2968001, 10328933832, ss2163920228, ss3687100787, ss5242851257, ss5443857050, ss5515442066	NC_000001.11:79615574:C:T	NC_000001.11:79615574: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 rs995513

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.
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dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs995513