Name: rs4072537
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.

rs4072537

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr1:1129916 (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
Variation Type: SNV Single Nucleotide Variation
Frequency: T=0.286811 (75916/264690, TOPMED)
T=0.294574 (41172/139768, GnomAD)
T=0.27071 (21304/78698, PAGE_STUDY) (+ 17 more)
T=0.30760 (12146/39486, ALFA)
T=0.40412 (11418/28254, 14KJPN)
T=0.40588 (6801/16756, 8.3KJPN)
T=0.2748 (1760/6404, 1000G_30x)
T=0.2778 (1391/5008, 1000G)
T=0.3366 (1508/4480, Estonian)
T=0.3142 (1211/3854, ALSPAC)
T=0.3193 (1184/3708, TWINSUK)
T=0.3962 (1161/2930, KOREAN)
T=0.3870 (709/1832, Korea1K)
T=0.335 (334/998, GoNL)
T=0.272 (163/600, NorthernSweden)
T=0.177 (91/514, SGDP_PRJ)
T=0.273 (59/216, Qatari)
T=0.383 (79/206, Vietnamese)
T=0.27 (13/48, Siberian)
T=0.38 (15/40, GENOME_DK)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: LOC124903820 : Intron Variant
LOC124903819 : 2KB Upstream 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	39580	T=0.30755	A=0.00000, C=0.69245
European	Sub	30418	T=0.31807	A=0.00000, C=0.68193
African	Sub	5736	T=0.2558	A=0.0000, C=0.7442
African Others	Sub	186	T=0.274	A=0.000, C=0.726
African American	Sub	5550	T=0.2551	A=0.0000, C=0.7449
Asian	Sub	162	T=0.426	A=0.000, C=0.574
East Asian	Sub	134	T=0.425	A=0.000, C=0.575
Other Asian	Sub	28	T=0.43	A=0.00, C=0.57
Latin American 1	Sub	168	T=0.250	A=0.000, C=0.750
Latin American 2	Sub	700	T=0.234	A=0.000, C=0.766
South Asian	Sub	120	T=0.258	A=0.000, C=0.742
Other	Sub	2276	T=0.3185	A=0.0000, C=0.6815

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=0.286811	C=0.713189
gnomAD - Genomes	Global	Study-wide	139768	T=0.294574	C=0.705426
gnomAD - Genomes	European	Sub	75726	T=0.32739	C=0.67261
gnomAD - Genomes	African	Sub	41846	T=0.23990	C=0.76010
gnomAD - Genomes	American	Sub	13618	T=0.25209	C=0.74791
gnomAD - Genomes	Ashkenazi Jewish	Sub	3324	T=0.3165	C=0.6835
gnomAD - Genomes	East Asian	Sub	3114	T=0.4004	C=0.5996
gnomAD - Genomes	Other	Sub	2140	T=0.2846	C=0.7154
The PAGE Study	Global	Study-wide	78698	T=0.27071	C=0.72929
The PAGE Study	AfricanAmerican	Sub	32514	T=0.24546	C=0.75454
The PAGE Study	Mexican	Sub	10810	T=0.25939	C=0.74061
The PAGE Study	Asian	Sub	8318	T=0.3961	C=0.6039
The PAGE Study	PuertoRican	Sub	7918	T=0.2584	C=0.7416
The PAGE Study	NativeHawaiian	Sub	4534	T=0.3341	C=0.6659
The PAGE Study	Cuban	Sub	4228	T=0.2888	C=0.7112
The PAGE Study	Dominican	Sub	3828	T=0.2495	C=0.7505
The PAGE Study	CentralAmerican	Sub	2450	T=0.2196	C=0.7804
The PAGE Study	SouthAmerican	Sub	1982	T=0.1786	C=0.8214
The PAGE Study	NativeAmerican	Sub	1260	T=0.2857	C=0.7143
The PAGE Study	SouthAsian	Sub	856	T=0.275	C=0.725
Allele Frequency Aggregator	Total	Global	39486	T=0.30760	A=0.00000, C=0.69240
Allele Frequency Aggregator	European	Sub	30342	T=0.31817	A=0.00000, C=0.68183
Allele Frequency Aggregator	African	Sub	5736	T=0.2558	A=0.0000, C=0.7442
Allele Frequency Aggregator	Other	Sub	2258	T=0.3184	A=0.0000, C=0.6816
Allele Frequency Aggregator	Latin American 2	Sub	700	T=0.234	A=0.000, C=0.766
Allele Frequency Aggregator	Latin American 1	Sub	168	T=0.250	A=0.000, C=0.750
Allele Frequency Aggregator	Asian	Sub	162	T=0.426	A=0.000, C=0.574
Allele Frequency Aggregator	South Asian	Sub	120	T=0.258	A=0.000, C=0.742
14KJPN	JAPANESE	Study-wide	28254	T=0.40412	C=0.59588
8.3KJPN	JAPANESE	Study-wide	16756	T=0.40588	C=0.59412
1000Genomes_30x	Global	Study-wide	6404	T=0.2748	C=0.7252
1000Genomes_30x	African	Sub	1786	T=0.2167	C=0.7833
1000Genomes_30x	Europe	Sub	1266	T=0.3002	C=0.6998
1000Genomes_30x	South Asian	Sub	1202	T=0.2554	C=0.7446
1000Genomes_30x	East Asian	Sub	1170	T=0.4026	C=0.5974
1000Genomes_30x	American	Sub	980	T=0.219	C=0.781
1000Genomes	Global	Study-wide	5008	T=0.2778	C=0.7222
1000Genomes	African	Sub	1322	T=0.2103	C=0.7897
1000Genomes	East Asian	Sub	1008	T=0.4107	C=0.5893
1000Genomes	Europe	Sub	1006	T=0.3022	C=0.6978
1000Genomes	South Asian	Sub	978	T=0.251	C=0.749
1000Genomes	American	Sub	694	T=0.216	C=0.784
Genetic variation in the Estonian population	Estonian	Study-wide	4480	T=0.3366	C=0.6634
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	T=0.3142	C=0.6858
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	T=0.3193	C=0.6807
KOREAN population from KRGDB	KOREAN	Study-wide	2930	T=0.3962	C=0.6038
Korean Genome Project	KOREAN	Study-wide	1832	T=0.3870	C=0.6130
Genome of the Netherlands Release 5	Genome of the Netherlands	Study-wide	998	T=0.335	C=0.665
Northern Sweden	ACPOP	Study-wide	600	T=0.272	C=0.728
SGDP_PRJ	Global	Study-wide	514	T=0.177	C=0.823
Qatari	Global	Study-wide	216	T=0.273	C=0.727
A Vietnamese Genetic Variation Database	Global	Study-wide	206	T=0.383	C=0.617
Siberian	Global	Study-wide	48	T=0.27	C=0.73
The Danish reference pan genome	Danish	Study-wide	40	T=0.38	C=0.62

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.1129916T>A
GRCh38.p14 chr 1	NC_000001.11:g.1129916T>C
GRCh37.p13 chr 1	NC_000001.10:g.1065296T>A
GRCh37.p13 chr 1	NC_000001.10:g.1065296T>C

Gene: LOC124903820, uncharacterized LOC124903820 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
LOC124903820 transcript variant X2	XR_007065351.1:n.	N/A	Intron Variant
LOC124903820 transcript variant X1	XR_007065350.1:n.	N/A	Genic Upstream Transcript Variant

Gene: LOC124903819, uncharacterized LOC124903819 (minus strand) : 2KB Upstream Variant

Molecule type	Change	Amino acid[Codon]	SO Term
LOC124903819 transcript	XR_007065349.1:n.	N/A	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.

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
GRCh38.p14 chr 1	NC_000001.11:g.1129916=	NC_000001.11:g.1129916T>A	NC_000001.11:g.1129916T>C
GRCh37.p13 chr 1	NC_000001.10:g.1065296=	NC_000001.10:g.1065296T>A	NC_000001.10:g.1065296T>C

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#.

110 SubSNP, 20 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	TSC-CSHL	ss5451735	Oct 10, 2002 (108)
2	SC_JCM	ss5872735	Feb 20, 2003 (111)
3	WI_SSAHASNP	ss11429401	Jul 11, 2003 (116)
4	SC_SNP	ss13052173	Dec 05, 2003 (119)
5	SC_SNP	ss14802091	Dec 05, 2003 (119)
6	CSHL-HAPMAP	ss16449596	Feb 27, 2004 (120)
7	CSHL-HAPMAP	ss19144803	Feb 27, 2004 (120)
8	SSAHASNP	ss20492342	Apr 05, 2004 (121)
9	PERLEGEN	ss23837051	Sep 20, 2004 (123)
10	ABI	ss41263063	Mar 14, 2006 (126)
11	ILLUMINA	ss67313547	Nov 30, 2006 (127)
12	ILLUMINA	ss67719643	Nov 30, 2006 (127)
13	ILLUMINA	ss68224896	Dec 12, 2006 (127)
14	PERLEGEN	ss68756319	May 17, 2007 (127)
15	KRIBB_YJKIM	ss84222327	Dec 15, 2007 (130)
16	HUMANGENOME_JCVI	ss99179778	Feb 05, 2009 (130)
17	BGI	ss102713640	Dec 01, 2009 (131)
18	1000GENOMES	ss107938581	Jan 22, 2009 (130)
19	1000GENOMES	ss109941484	Jan 24, 2009 (130)
20	ILLUMINA-UK	ss118440213	Dec 01, 2009 (131)
21	ENSEMBL	ss131634225	Dec 01, 2009 (131)
22	COMPLETE_GENOMICS	ss162983560	Jul 04, 2010 (132)
23	COMPLETE_GENOMICS	ss163707724	Jul 04, 2010 (132)
24	COMPLETE_GENOMICS	ss165982781	Jul 04, 2010 (132)
25	BUSHMAN	ss197889034	Jul 04, 2010 (132)
26	BCM-HGSC-SUB	ss205393032	Jul 04, 2010 (132)
27	1000GENOMES	ss218191985	Jul 14, 2010 (132)
28	1000GENOMES	ss230396480	Jul 14, 2010 (132)
29	1000GENOMES	ss238116031	Jul 15, 2010 (132)
30	BL	ss252866308	May 09, 2011 (134)
31	GMI	ss275682500	May 04, 2012 (137)
32	GMI	ss283988016	Apr 25, 2013 (138)
33	PJP	ss290494378	May 09, 2011 (134)
34	ILLUMINA	ss482054544	May 04, 2012 (137)
35	ILLUMINA	ss484192707	May 04, 2012 (137)
36	ILLUMINA	ss536380737	Sep 08, 2015 (146)
37	TISHKOFF	ss553713731	Apr 25, 2013 (138)
38	SSMP	ss647518494	Apr 25, 2013 (138)
39	ILLUMINA	ss780561614	Aug 21, 2014 (142)
40	ILLUMINA	ss782542280	Aug 21, 2014 (142)
41	ILLUMINA	ss836053890	Aug 21, 2014 (142)
42	EVA-GONL	ss974772125	Aug 21, 2014 (142)
43	JMKIDD_LAB	ss1067613767	Aug 21, 2014 (142)
44	1000GENOMES	ss1289350804	Aug 21, 2014 (142)
45	DDI	ss1425685898	Apr 01, 2015 (144)
46	EVA_GENOME_DK	ss1573852069	Apr 01, 2015 (144)
47	EVA_DECODE	ss1584132043	Apr 01, 2015 (144)
48	EVA_UK10K_ALSPAC	ss1599382825	Apr 01, 2015 (144)
49	EVA_UK10K_TWINSUK	ss1642376858	Apr 01, 2015 (144)
50	HAMMER_LAB	ss1793717203	Sep 08, 2015 (146)
51	WEILL_CORNELL_DGM	ss1917964033	Feb 12, 2016 (147)
52	ILLUMINA	ss1958230808	Feb 12, 2016 (147)
53	GENOMED	ss1966667752	Jul 19, 2016 (147)
54	JJLAB	ss2019499899	Sep 14, 2016 (149)
55	USC_VALOUEV	ss2147486684	Dec 20, 2016 (150)
56	HUMAN_LONGEVITY	ss2159387227	Dec 20, 2016 (150)
57	SYSTEMSBIOZJU	ss2624265575	Nov 08, 2017 (151)
58	ILLUMINA	ss2632465759	Nov 08, 2017 (151)
59	GRF	ss2697377609	Nov 08, 2017 (151)
60	GNOMAD	ss2750673241	Nov 08, 2017 (151)
61	AFFY	ss2984841255	Nov 08, 2017 (151)
62	AFFY	ss2985495011	Nov 08, 2017 (151)
63	SWEGEN	ss2986154554	Nov 08, 2017 (151)
64	ILLUMINA	ss3021043761	Nov 08, 2017 (151)
65	BIOINF_KMB_FNS_UNIBA	ss3023514331	Nov 08, 2017 (151)
66	CSHL	ss3343274355	Nov 08, 2017 (151)
67	ILLUMINA	ss3626007119	Oct 11, 2018 (152)
68	ILLUMINA	ss3630505795	Oct 11, 2018 (152)
69	ILLUMINA	ss3638887872	Oct 11, 2018 (152)
70	ILLUMINA	ss3639756841	Oct 11, 2018 (152)
71	ILLUMINA	ss3641566338	Oct 11, 2018 (152)
72	ILLUMINA	ss3643810772	Oct 11, 2018 (152)
73	URBANLAB	ss3646581968	Oct 11, 2018 (152)
74	ILLUMINA	ss3651365813	Oct 11, 2018 (152)
75	ILLUMINA	ss3653615019	Oct 11, 2018 (152)
76	EGCUT_WGS	ss3654265666	Jul 12, 2019 (153)
77	EVA_DECODE	ss3685998235	Jul 12, 2019 (153)
78	ILLUMINA	ss3724988478	Jul 12, 2019 (153)
79	ACPOP	ss3726718810	Jul 12, 2019 (153)
80	EVA	ss3745724457	Jul 12, 2019 (153)
81	PAGE_CC	ss3770778842	Jul 12, 2019 (153)
82	PACBIO	ss3783303055	Jul 12, 2019 (153)
83	PACBIO	ss3788980829	Jul 12, 2019 (153)
84	PACBIO	ss3793853378	Jul 12, 2019 (153)
85	KHV_HUMAN_GENOMES	ss3798747061	Jul 12, 2019 (153)
86	EVA	ss3825982672	Apr 25, 2020 (154)
87	EVA	ss3836379034	Apr 25, 2020 (154)
88	EVA	ss3841783061	Apr 25, 2020 (154)
89	SGDP_PRJ	ss3848004258	Apr 25, 2020 (154)
90	KRGDB	ss3892847101	Apr 25, 2020 (154)
91	KOGIC	ss3943636606	Apr 25, 2020 (154)
92	TOPMED	ss4436524007	Apr 25, 2021 (155)
93	TOMMO_GENOMICS	ss5142067481	Apr 25, 2021 (155)
94	1000G_HIGH_COVERAGE	ss5240874026	Oct 12, 2022 (156)
95	EVA	ss5314586053	Oct 12, 2022 (156)
96	EVA	ss5316200764	Oct 12, 2022 (156)
97	HUGCELL_USP	ss5442120746	Oct 12, 2022 (156)
98	1000G_HIGH_COVERAGE	ss5512502966	Oct 12, 2022 (156)
99	SANFORD_IMAGENETICS	ss5624193883	Oct 12, 2022 (156)
100	SANFORD_IMAGENETICS	ss5624755640	Oct 12, 2022 (156)
101	TOMMO_GENOMICS	ss5666212226	Oct 12, 2022 (156)
102	YY_MCH	ss5800246442	Oct 12, 2022 (156)
103	EVA	ss5831423052	Oct 12, 2022 (156)
104	EVA	ss5847150770	Oct 12, 2022 (156)
105	EVA	ss5847521469	Oct 12, 2022 (156)
106	EVA	ss5848749808	Oct 12, 2022 (156)
107	EVA	ss5906715453	Oct 12, 2022 (156)
108	EVA	ss5936587880	Oct 12, 2022 (156)
109	EVA	ss5979259885	Oct 12, 2022 (156)
110	EVA	ss5979926492	Oct 12, 2022 (156)
111	1000Genomes	NC_000001.10 - 1065296	Oct 11, 2018 (152)
112	1000Genomes_30x	NC_000001.11 - 1129916	Oct 12, 2022 (156)
113	The Avon Longitudinal Study of Parents and Children	NC_000001.10 - 1065296	Oct 11, 2018 (152)
114	Genetic variation in the Estonian population	NC_000001.10 - 1065296	Oct 11, 2018 (152)
115	The Danish reference pan genome	NC_000001.10 - 1065296	Apr 25, 2020 (154)
116	gnomAD - Genomes	NC_000001.11 - 1129916	Apr 25, 2021 (155)
117	Genome of the Netherlands Release 5	NC_000001.10 - 1065296	Apr 25, 2020 (154)
118	KOREAN population from KRGDB	NC_000001.10 - 1065296	Apr 25, 2020 (154)
119	Korean Genome Project	NC_000001.11 - 1129916	Apr 25, 2020 (154)
120	Northern Sweden	NC_000001.10 - 1065296	Jul 12, 2019 (153)
121	The PAGE Study	NC_000001.11 - 1129916	Jul 12, 2019 (153)
122	Qatari	NC_000001.10 - 1065296	Apr 25, 2020 (154)
123	SGDP_PRJ	NC_000001.10 - 1065296	Apr 25, 2020 (154)
124	Siberian	NC_000001.10 - 1065296	Apr 25, 2020 (154)
125	8.3KJPN	NC_000001.10 - 1065296	Apr 25, 2021 (155)
126	14KJPN	NC_000001.11 - 1129916	Oct 12, 2022 (156)
127	TopMed	NC_000001.11 - 1129916	Apr 25, 2021 (155)
128	UK 10K study - Twins	NC_000001.10 - 1065296	Oct 11, 2018 (152)
129	A Vietnamese Genetic Variation Database	NC_000001.10 - 1065296	Jul 12, 2019 (153)
130	ALFA	NC_000001.11 - 1129916	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)
rs34813285	Oct 15, 2006 (127)
rs58516161	May 24, 2008 (130)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
11091397264	NC_000001.11:1129915:T:A	NC_000001.11:1129915:T:A	(self)
ss3638887872, ss3639756841, ss3643810772	NC_000001.8:1105218:T:C	NC_000001.11:1129915:T:C	(self)
ss107938581, ss109941484, ss118440213, ss162983560, ss163707724, ss165982781, ss197889034, ss205393032, ss252866308, ss275682500, ss283988016, ss290494378, ss482054544, ss1584132043	NC_000001.9:1055158:T:C	NC_000001.11:1129915:T:C	(self)
15943, 5225, 3914, 1359303, 2403, 24495, 3675, 5963, 21238, 3038, 36788, 5225, 1164, ss218191985, ss230396480, ss238116031, ss484192707, ss536380737, ss553713731, ss647518494, ss780561614, ss782542280, ss836053890, ss974772125, ss1067613767, ss1289350804, ss1425685898, ss1573852069, ss1599382825, ss1642376858, ss1793717203, ss1917964033, ss1958230808, ss1966667752, ss2019499899, ss2147486684, ss2624265575, ss2632465759, ss2697377609, ss2750673241, ss2984841255, ss2985495011, ss2986154554, ss3021043761, ss3343274355, ss3626007119, ss3630505795, ss3641566338, ss3651365813, ss3653615019, ss3654265666, ss3726718810, ss3745724457, ss3783303055, ss3788980829, ss3793853378, ss3825982672, ss3836379034, ss3848004258, ss3892847101, ss5142067481, ss5314586053, ss5316200764, ss5624193883, ss5624755640, ss5831423052, ss5847150770, ss5847521469, ss5936587880, ss5979259885, ss5979926492	NC_000001.10:1065295:T:C	NC_000001.11:1129915:T:C	(self)
28901, 145250, 14607, 311, 49330, 130342, 11091397264, ss2159387227, ss3023514331, ss3646581968, ss3685998235, ss3724988478, ss3770778842, ss3798747061, ss3841783061, ss3943636606, ss4436524007, ss5240874026, ss5442120746, ss5512502966, ss5666212226, ss5800246442, ss5848749808, ss5906715453	NC_000001.11:1129915:T:C	NC_000001.11:1129915:T:C	(self)
ss5451735, ss5872735, ss14802091, ss23837051, ss41263063, ss67313547, ss67719643, ss68224896, ss68756319, ss84222327, ss99179778, ss102713640, ss131634225	NT_004350.19:543927:T:C	NC_000001.11:1129915:T:C	(self)
ss16449596, ss19144803, ss20492342	NT_077913.2:69006:T:C	NC_000001.11:1129915:T:C	(self)
ss11429401, ss13052173	NT_077960.1:134736:T:C	NC_000001.11:1129915:T:C	(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 rs4072537

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

rs4072537