Name: rs2633716
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.

rs2633716

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr3:4786729 (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: T>A / T>C / T>G
Variation Type: SNV Single Nucleotide Variation
Frequency: T=0.070365 (18625/264690, TOPMED)
T=0.068106 (9547/140178, GnomAD)
T=0.00000 (0/28258, 14KJPN) (+ 19 more)
T=0.05444 (1206/22152, ALFA)
T=0.00000 (0/16760, 8.3KJPN)
T=0.0707 (453/6404, 1000G_30x)
T=0.0669 (335/5008, 1000G)
T=0.0158 (71/4480, Estonian)
T=0.0221 (85/3854, ALSPAC)
T=0.0299 (111/3708, TWINSUK)
T=0.0000 (0/2930, KOREAN)
A=0.0000 (0/2930, KOREAN)
C=0.0000 (0/2930, KOREAN)
T=0.0000 (0/1832, Korea1K)
T=0.0806 (139/1724, HapMap)
T=0.029 (29/998, GoNL)
T=0.025 (15/600, NorthernSweden)
T=0.022 (12/556, SGDP_PRJ)
T=0.106 (23/216, Qatari)
T=0.005 (1/212, Vietnamese)
T=0.00 (0/56, Siberian)
T=0.05 (2/40, GENOME_DK)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: ITPR1 : 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	22152	T=0.05444	G=0.94556
European	Sub	15966	T=0.02593	G=0.97407
African	Sub	4114	T=0.1723	G=0.8277
African Others	Sub	148	T=0.250	G=0.750
African American	Sub	3966	T=0.1694	G=0.8306
Asian	Sub	124	T=0.008	G=0.992
East Asian	Sub	96	T=0.01	G=0.99
Other Asian	Sub	28	T=0.00	G=1.00
Latin American 1	Sub	168	T=0.065	G=0.935
Latin American 2	Sub	670	T=0.024	G=0.976
South Asian	Sub	98	T=0.02	G=0.98
Other	Sub	1012	T=0.0524	G=0.9476

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	T=0.070365	G=0.929635
gnomAD - Genomes	Global	Study-wide	140178	T=0.068106	G=0.931894
gnomAD - Genomes	European	Sub	75940	T=0.02760	G=0.97240
gnomAD - Genomes	African	Sub	41966	T=0.15925	G=0.84075
gnomAD - Genomes	American	Sub	13666	T=0.03234	G=0.96766
gnomAD - Genomes	Ashkenazi Jewish	Sub	3324	T=0.0590	G=0.9410
gnomAD - Genomes	East Asian	Sub	3132	T=0.0013	G=0.9987
gnomAD - Genomes	Other	Sub	2150	T=0.0586	G=0.9414
14KJPN	JAPANESE	Study-wide	28258	T=0.00000	G=1.00000
Allele Frequency Aggregator	Total	Global	22152	T=0.05444	G=0.94556
Allele Frequency Aggregator	European	Sub	15966	T=0.02593	G=0.97407
Allele Frequency Aggregator	African	Sub	4114	T=0.1723	G=0.8277
Allele Frequency Aggregator	Other	Sub	1012	T=0.0524	G=0.9476
Allele Frequency Aggregator	Latin American 2	Sub	670	T=0.024	G=0.976
Allele Frequency Aggregator	Latin American 1	Sub	168	T=0.065	G=0.935
Allele Frequency Aggregator	Asian	Sub	124	T=0.008	G=0.992
Allele Frequency Aggregator	South Asian	Sub	98	T=0.02	G=0.98
8.3KJPN	JAPANESE	Study-wide	16760	T=0.00000	G=1.00000
1000Genomes_30x	Global	Study-wide	6404	T=0.0707	G=0.9293
1000Genomes_30x	African	Sub	1786	T=0.1865	G=0.8135
1000Genomes_30x	Europe	Sub	1266	T=0.0434	G=0.9566
1000Genomes_30x	South Asian	Sub	1202	T=0.0200	G=0.9800
1000Genomes_30x	East Asian	Sub	1170	T=0.0026	G=0.9974
1000Genomes_30x	American	Sub	980	T=0.039	G=0.961
1000Genomes	Global	Study-wide	5008	T=0.0669	G=0.9331
1000Genomes	African	Sub	1322	T=0.1868	G=0.8132
1000Genomes	East Asian	Sub	1008	T=0.0030	G=0.9970
1000Genomes	Europe	Sub	1006	T=0.0388	G=0.9612
1000Genomes	South Asian	Sub	978	T=0.019	G=0.981
1000Genomes	American	Sub	694	T=0.039	G=0.961
Genetic variation in the Estonian population	Estonian	Study-wide	4480	T=0.0158	G=0.9842
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	T=0.0221	G=0.9779
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	T=0.0299	G=0.9701
KOREAN population from KRGDB	KOREAN	Study-wide	2930	T=0.0000	A=0.0000, C=0.0000, G=1.0000
Korean Genome Project	KOREAN	Study-wide	1832	T=0.0000	G=1.0000
HapMap	Global	Study-wide	1724	T=0.0806	G=0.9194
HapMap	American	Sub	770	T=0.045	G=0.955
HapMap	African	Sub	690	T=0.142	G=0.858
HapMap	Europe	Sub	174	T=0.034	G=0.966
HapMap	Asian	Sub	90	T=0.00	G=1.00
Genome of the Netherlands Release 5	Genome of the Netherlands	Study-wide	998	T=0.029	G=0.971
Northern Sweden	ACPOP	Study-wide	600	T=0.025	G=0.975
SGDP_PRJ	Global	Study-wide	556	T=0.022	G=0.978
Qatari	Global	Study-wide	216	T=0.106	G=0.894
A Vietnamese Genetic Variation Database	Global	Study-wide	212	T=0.005	G=0.995
Siberian	Global	Study-wide	56	T=0.00	G=1.00
The Danish reference pan genome	Danish	Study-wide	40	T=0.05	G=0.95

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 3	NC_000003.12:g.4786729T>A
GRCh38.p14 chr 3	NC_000003.12:g.4786729T>C
GRCh38.p14 chr 3	NC_000003.12:g.4786729T>G
GRCh37.p13 chr 3	NC_000003.11:g.4828413T>A
GRCh37.p13 chr 3	NC_000003.11:g.4828413T>C
GRCh37.p13 chr 3	NC_000003.11:g.4828413T>G
ITPR1 RefSeqGene	NG_016144.1:g.298382T>A
ITPR1 RefSeqGene	NG_016144.1:g.298382T>C
ITPR1 RefSeqGene	NG_016144.1:g.298382T>G

Gene: ITPR1, inositol 1,4,5-trisphosphate receptor type 1 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
ITPR1 transcript variant 1	NM_001099952.4:c.6472-121… NM_001099952.4:c.6472-1218T>A	N/A	Intron Variant
ITPR1 transcript variant 3	NM_001168272.2:c.6571-121… NM_001168272.2:c.6571-1218T>A	N/A	Intron Variant
ITPR1 transcript variant 4	NM_001378452.1:c.6616-121… NM_001378452.1:c.6616-1218T>A	N/A	Intron Variant
ITPR1 transcript variant 2	NM_002222.7:c.6427-1218T>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	T=	A	C	G
GRCh38.p14 chr 3	NC_000003.12:g.4786729=	NC_000003.12:g.4786729T>A	NC_000003.12:g.4786729T>C	NC_000003.12:g.4786729T>G
GRCh37.p13 chr 3	NC_000003.11:g.4828413=	NC_000003.11:g.4828413T>A	NC_000003.11:g.4828413T>C	NC_000003.11:g.4828413T>G
ITPR1 RefSeqGene	NG_016144.1:g.298382=	NG_016144.1:g.298382T>A	NG_016144.1:g.298382T>C	NG_016144.1:g.298382T>G
ITPR1 transcript variant 1	NM_001099952.2:c.6472-1218=	NM_001099952.2:c.6472-1218T>A	NM_001099952.2:c.6472-1218T>C	NM_001099952.2:c.6472-1218T>G
ITPR1 transcript variant 1	NM_001099952.4:c.6472-1218=	NM_001099952.4:c.6472-1218T>A	NM_001099952.4:c.6472-1218T>C	NM_001099952.4:c.6472-1218T>G
ITPR1 transcript variant 3	NM_001168272.1:c.6571-1218=	NM_001168272.1:c.6571-1218T>A	NM_001168272.1:c.6571-1218T>C	NM_001168272.1:c.6571-1218T>G
ITPR1 transcript variant 3	NM_001168272.2:c.6571-1218=	NM_001168272.2:c.6571-1218T>A	NM_001168272.2:c.6571-1218T>C	NM_001168272.2:c.6571-1218T>G
ITPR1 transcript variant 4	NM_001378452.1:c.6616-1218=	NM_001378452.1:c.6616-1218T>A	NM_001378452.1:c.6616-1218T>C	NM_001378452.1:c.6616-1218T>G
ITPR1 transcript variant 2	NM_002222.5:c.6427-1218=	NM_002222.5:c.6427-1218T>A	NM_002222.5:c.6427-1218T>C	NM_002222.5:c.6427-1218T>G
ITPR1 transcript variant 2	NM_002222.7:c.6427-1218=	NM_002222.7:c.6427-1218T>A	NM_002222.7:c.6427-1218T>C	NM_002222.7:c.6427-1218T>G
ITPR1 transcript variant X1	XM_005265108.1:c.6619-1218=	XM_005265108.1:c.6619-1218T>A	XM_005265108.1:c.6619-1218T>C	XM_005265108.1:c.6619-1218T>G
ITPR1 transcript variant X2	XM_005265109.1:c.6547-1218=	XM_005265109.1:c.6547-1218T>A	XM_005265109.1:c.6547-1218T>C	XM_005265109.1:c.6547-1218T>G
ITPR1 transcript variant X3	XM_005265110.1:c.6499-1218=	XM_005265110.1:c.6499-1218T>A	XM_005265110.1:c.6499-1218T>C	XM_005265110.1:c.6499-1218T>G

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#.

89 SubSNP, 20 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	SC_JCM	ss3709690	Sep 28, 2001 (100)
2	CSHL-HAPMAP	ss19515550	Feb 27, 2004 (120)
3	SSAHASNP	ss21941924	Apr 05, 2004 (121)
4	ABI	ss44407830	Mar 15, 2006 (126)
5	ILLUMINA	ss65791486	Oct 15, 2006 (127)
6	ILLUMINA	ss74885826	Dec 07, 2007 (129)
7	HGSV	ss77520413	Dec 07, 2007 (129)
8	HGSV	ss78379538	Dec 07, 2007 (129)
9	HGSV	ss79972329	Dec 15, 2007 (130)
10	BCMHGSC_JDW	ss91978061	Mar 24, 2008 (129)
11	HUMANGENOME_JCVI	ss99071858	Feb 06, 2009 (130)
12	BGI	ss106237944	Feb 06, 2009 (130)
13	1000GENOMES	ss111159760	Jan 25, 2009 (130)
14	1000GENOMES	ss111995396	Jan 25, 2009 (130)
15	ILLUMINA-UK	ss116953025	Feb 14, 2009 (130)
16	KRIBB_YJKIM	ss119441137	Dec 01, 2009 (131)
17	ENSEMBL	ss135313425	Dec 01, 2009 (131)
18	ENSEMBL	ss138691713	Dec 01, 2009 (131)
19	GMI	ss155033385	Dec 01, 2009 (131)
20	COMPLETE_GENOMICS	ss161901803	Jul 04, 2010 (132)
21	COMPLETE_GENOMICS	ss163036375	Jul 04, 2010 (132)
22	COMPLETE_GENOMICS	ss166066500	Jul 04, 2010 (132)
23	ILLUMINA	ss173413916	Jul 04, 2010 (132)
24	BUSHMAN	ss202058872	Jul 04, 2010 (132)
25	BCM-HGSC-SUB	ss206007469	Jul 04, 2010 (132)
26	1000GENOMES	ss219949244	Jul 14, 2010 (132)
27	1000GENOMES	ss231684835	Jul 14, 2010 (132)
28	1000GENOMES	ss239123105	Jul 15, 2010 (132)
29	BL	ss252897064	May 09, 2011 (134)
30	GMI	ss276991082	May 04, 2012 (137)
31	GMI	ss284583932	Apr 25, 2013 (138)
32	PJP	ss292786369	May 09, 2011 (134)
33	ILLUMINA	ss537111056	Sep 08, 2015 (146)
34	TISHKOFF	ss556387386	Apr 25, 2013 (138)
35	SSMP	ss650051141	Apr 25, 2013 (138)
36	EVA-GONL	ss978213294	Aug 21, 2014 (142)
37	JMKIDD_LAB	ss1070129975	Aug 21, 2014 (142)
38	1000GENOMES	ss1302585741	Aug 21, 2014 (142)
39	DDI	ss1429312304	Apr 01, 2015 (144)
40	EVA_GENOME_DK	ss1579821134	Apr 01, 2015 (144)
41	EVA_DECODE	ss1587673140	Apr 01, 2015 (144)
42	EVA_UK10K_ALSPAC	ss1606298581	Apr 01, 2015 (144)
43	EVA_UK10K_TWINSUK	ss1649292614	Apr 01, 2015 (144)
44	EVA_SVP	ss1712549031	Apr 01, 2015 (144)
45	HAMMER_LAB	ss1798768507	Sep 08, 2015 (146)
46	WEILL_CORNELL_DGM	ss1921465449	Feb 12, 2016 (147)
47	GENOMED	ss1969308905	Jul 19, 2016 (147)
48	JJLAB	ss2021283778	Sep 14, 2016 (149)
49	USC_VALOUEV	ss2149351246	Dec 20, 2016 (150)
50	HUMAN_LONGEVITY	ss2248646380	Dec 20, 2016 (150)
51	SYSTEMSBIOZJU	ss2625141761	Nov 08, 2017 (151)
52	GRF	ss2704708152	Nov 08, 2017 (151)
53	GNOMAD	ss2788941690	Nov 08, 2017 (151)
54	SWEGEN	ss2991743600	Nov 08, 2017 (151)
55	BIOINF_KMB_FNS_UNIBA	ss3024403904	Nov 08, 2017 (151)
56	CSHL	ss3344857651	Nov 08, 2017 (151)
57	ILLUMINA	ss3628576449	Oct 11, 2018 (152)
58	ILLUMINA	ss3638393752	Oct 11, 2018 (152)
59	ILLUMINA	ss3643352410	Oct 11, 2018 (152)
60	URBANLAB	ss3647328928	Oct 11, 2018 (152)
61	EGCUT_WGS	ss3659641084	Jul 13, 2019 (153)
62	EVA_DECODE	ss3708531249	Jul 13, 2019 (153)
63	ACPOP	ss3729584189	Jul 13, 2019 (153)
64	EVA	ss3759591969	Jul 13, 2019 (153)
65	PACBIO	ss3784219888	Jul 13, 2019 (153)
66	PACBIO	ss3789750508	Jul 13, 2019 (153)
67	PACBIO	ss3794624229	Jul 13, 2019 (153)
68	KHV_HUMAN_GENOMES	ss3802742855	Jul 13, 2019 (153)
69	EVA	ss3827632469	Apr 25, 2020 (154)
70	EVA	ss3837237588	Apr 25, 2020 (154)
71	EVA	ss3842661142	Apr 25, 2020 (154)
72	SGDP_PRJ	ss3855109867	Apr 25, 2020 (154)
73	KRGDB	ss3900875574	Apr 25, 2020 (154)
74	KOGIC	ss3950560461	Apr 25, 2020 (154)
75	EVA	ss4017061806	Apr 27, 2021 (155)
76	TOPMED	ss4552447703	Apr 27, 2021 (155)
77	TOMMO_GENOMICS	ss5157561609	Apr 27, 2021 (155)
78	1000G_HIGH_COVERAGE	ss5252859977	Oct 13, 2022 (156)
79	EVA	ss5337545567	Oct 13, 2022 (156)
80	HUGCELL_USP	ss5452382865	Oct 13, 2022 (156)
81	1000G_HIGH_COVERAGE	ss5530600354	Oct 13, 2022 (156)
82	SANFORD_IMAGENETICS	ss5631432120	Oct 13, 2022 (156)
83	TOMMO_GENOMICS	ss5688762602	Oct 13, 2022 (156)
84	YY_MCH	ss5803432611	Oct 13, 2022 (156)
85	EVA	ss5825271825	Oct 13, 2022 (156)
86	EVA	ss5853465579	Oct 13, 2022 (156)
87	EVA	ss5867413834	Oct 13, 2022 (156)
88	EVA	ss5959688757	Oct 13, 2022 (156)
89	EVA	ss5980127461	Oct 13, 2022 (156)
90	1000Genomes	NC_000003.11 - 4828413	Oct 11, 2018 (152)
91	1000Genomes_30x	NC_000003.12 - 4786729	Oct 13, 2022 (156)
92	The Avon Longitudinal Study of Parents and Children	NC_000003.11 - 4828413	Oct 11, 2018 (152)
93	Genetic variation in the Estonian population	NC_000003.11 - 4828413	Oct 11, 2018 (152)
94	The Danish reference pan genome	NC_000003.11 - 4828413	Apr 25, 2020 (154)
95	gnomAD - Genomes	NC_000003.12 - 4786729	Apr 27, 2021 (155)
96	Genome of the Netherlands Release 5	NC_000003.11 - 4828413	Apr 25, 2020 (154)
97	HapMap	NC_000003.12 - 4786729	Apr 25, 2020 (154)
98	KOREAN population from KRGDB	NC_000003.11 - 4828413	Apr 25, 2020 (154)
99	Korean Genome Project	NC_000003.12 - 4786729	Apr 25, 2020 (154)
100	Northern Sweden	NC_000003.11 - 4828413	Jul 13, 2019 (153)
101	Qatari	NC_000003.11 - 4828413	Apr 25, 2020 (154)
102	SGDP_PRJ	NC_000003.11 - 4828413	Apr 25, 2020 (154)
103	Siberian	NC_000003.11 - 4828413	Apr 25, 2020 (154)
104	8.3KJPN	NC_000003.11 - 4828413	Apr 27, 2021 (155)
105	14KJPN	NC_000003.12 - 4786729	Oct 13, 2022 (156)
106	TopMed	NC_000003.12 - 4786729	Apr 27, 2021 (155)
107	UK 10K study - Twins	NC_000003.11 - 4828413	Oct 11, 2018 (152)
108	A Vietnamese Genetic Variation Database	NC_000003.11 - 4828413	Jul 13, 2019 (153)
109	ALFA	NC_000003.12 - 4786729	Apr 27, 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)
rs60756024	May 26, 2008 (130)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
8052968, ss3900875574	NC_000003.11:4828412:T:A	NC_000003.12:4786728:T:A	(self)
ss2248646380	NC_000003.12:4786728:T:A	NC_000003.12:4786728:T:A	(self)
8052968, ss3900875574	NC_000003.11:4828412:T:C	NC_000003.12:4786728:T:C	(self)
ss77520413, ss78379538, ss79972329	NC_000003.9:4803412:T:G	NC_000003.12:4786728:T:G	(self)
ss91978061, ss111159760, ss111995396, ss116953025, ss161901803, ss163036375, ss166066500, ss202058872, ss206007469, ss252897064, ss276991082, ss284583932, ss292786369, ss1587673140, ss1712549031, ss3643352410	NC_000003.10:4803412:T:G	NC_000003.12:4786728:T:G	(self)
13723570, 7605344, 5379332, 5986073, 3337498, 8052968, 2869054, 3507379, 7126847, 1867600, 15530916, 7605344, 1654693, ss219949244, ss231684835, ss239123105, ss537111056, ss556387386, ss650051141, ss978213294, ss1070129975, ss1302585741, ss1429312304, ss1579821134, ss1606298581, ss1649292614, ss1798768507, ss1921465449, ss1969308905, ss2021283778, ss2149351246, ss2625141761, ss2704708152, ss2788941690, ss2991743600, ss3344857651, ss3628576449, ss3638393752, ss3659641084, ss3729584189, ss3759591969, ss3784219888, ss3789750508, ss3794624229, ss3827632469, ss3837237588, ss3855109867, ss3900875574, ss4017061806, ss5157561609, ss5337545567, ss5631432120, ss5825271825, ss5959688757, ss5980127461	NC_000003.11:4828412:T:G	NC_000003.12:4786728:T:G	(self)
18126289, 97542742, 2291628, 6938462, 22599706, 389825258, 5882489123, ss2248646380, ss3024403904, ss3647328928, ss3708531249, ss3802742855, ss3842661142, ss3950560461, ss4552447703, ss5252859977, ss5452382865, ss5530600354, ss5688762602, ss5803432611, ss5853465579, ss5867413834	NC_000003.12:4786728:T:G	NC_000003.12:4786728:T:G	(self)
ss19515550, ss21941924	NT_022517.16:4768412:T:G	NC_000003.12:4786728:T:G	(self)
ss3709690, ss44407830, ss65791486, ss74885826, ss99071858, ss106237944, ss119441137, ss135313425, ss138691713, ss155033385, ss173413916	NT_022517.18:4768412:T:G	NC_000003.12:4786728:T:G	(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 rs2633716

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

rs2633716