Name: rs1429138
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.

rs1429138

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr4:147361190 (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=0.062575 (16563/264690, TOPMED)
T=0.046388 (9513/205076, GENOGRAPHIC)
T=0.056687 (7949/140226, GnomAD) (+ 21 more)
T=0.04767 (3093/64884, ALFA)
T=0.21364 (6037/28258, 14KJPN)
T=0.21229 (3558/16760, 8.3KJPN)
T=0.0948 (607/6404, 1000G_30x)
T=0.0994 (498/5008, 1000G)
T=0.0344 (154/4480, Estonian)
T=0.0330 (127/3854, ALSPAC)
T=0.0380 (141/3708, TWINSUK)
T=0.1556 (456/2930, KOREAN)
T=0.1114 (232/2082, HGDP_Stanford)
T=0.1017 (190/1868, HapMap)
T=0.1556 (285/1832, Korea1K)
T=0.030 (30/998, GoNL)
T=0.122 (96/788, PRJEB37584)
T=0.017 (10/600, NorthernSweden)
T=0.097 (53/546, SGDP_PRJ)
T=0.162 (35/216, Qatari)
T=0.285 (61/214, Vietnamese)
T=0.06 (4/68, Ancient Sardinia)
T=0.04 (2/56, Siberian)
T=0.00 (0/40, 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	64884	T=0.04767	A=0.00000, C=0.95233
European	Sub	49552	T=0.03629	A=0.00000, C=0.96371
African	Sub	5460	T=0.0815	A=0.0000, C=0.9185
African Others	Sub	158	T=0.095	A=0.000, C=0.905
African American	Sub	5302	T=0.0811	A=0.0000, C=0.9189
Asian	Sub	134	T=0.239	A=0.000, C=0.761
East Asian	Sub	84	T=0.27	A=0.00, C=0.73
Other Asian	Sub	50	T=0.18	A=0.00, C=0.82
Latin American 1	Sub	260	T=0.062	A=0.000, C=0.938
Latin American 2	Sub	2784	T=0.0805	A=0.0000, C=0.9195
South Asian	Sub	4876	T=0.0913	A=0.0000, C=0.9087
Other	Sub	1818	T=0.0732	A=0.0000, C=0.9268

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").

Download

Study	Population	Group	Sample Size	Ref Allele	Alt Allele
TopMed	Global	Study-wide	264690	T=0.062575	C=0.937425
Genographic Project	Global	Study-wide	205076	T=0.046388	A=0.000000, C=0.953612
gnomAD - Genomes	Global	Study-wide	140226	T=0.056687	C=0.943313
gnomAD - Genomes	European	Sub	75956	T=0.03852	C=0.96148
gnomAD - Genomes	African	Sub	42018	T=0.07535	C=0.92465
gnomAD - Genomes	American	Sub	13654	T=0.06767	C=0.93233
gnomAD - Genomes	Ashkenazi Jewish	Sub	3324	T=0.0599	C=0.9401
gnomAD - Genomes	East Asian	Sub	3126	T=0.1839	C=0.8161
gnomAD - Genomes	Other	Sub	2148	T=0.0740	C=0.9260
Allele Frequency Aggregator	Total	Global	64884	T=0.04767	A=0.00000, C=0.95233
Allele Frequency Aggregator	European	Sub	49552	T=0.03629	A=0.00000, C=0.96371
Allele Frequency Aggregator	African	Sub	5460	T=0.0815	A=0.0000, C=0.9185
Allele Frequency Aggregator	South Asian	Sub	4876	T=0.0913	A=0.0000, C=0.9087
Allele Frequency Aggregator	Latin American 2	Sub	2784	T=0.0805	A=0.0000, C=0.9195
Allele Frequency Aggregator	Other	Sub	1818	T=0.0732	A=0.0000, C=0.9268
Allele Frequency Aggregator	Latin American 1	Sub	260	T=0.062	A=0.000, C=0.938
Allele Frequency Aggregator	Asian	Sub	134	T=0.239	A=0.000, C=0.761
14KJPN	JAPANESE	Study-wide	28258	T=0.21364	C=0.78636
8.3KJPN	JAPANESE	Study-wide	16760	T=0.21229	C=0.78771
1000Genomes_30x	Global	Study-wide	6404	T=0.0948	C=0.9052
1000Genomes_30x	African	Sub	1786	T=0.0683	C=0.9317
1000Genomes_30x	Europe	Sub	1266	T=0.0442	C=0.9558
1000Genomes_30x	South Asian	Sub	1202	T=0.0824	C=0.9176
1000Genomes_30x	East Asian	Sub	1170	T=0.2120	C=0.7880
1000Genomes_30x	American	Sub	980	T=0.084	C=0.916
1000Genomes	Global	Study-wide	5008	T=0.0994	C=0.9006
1000Genomes	African	Sub	1322	T=0.0756	C=0.9244
1000Genomes	East Asian	Sub	1008	T=0.2153	C=0.7847
1000Genomes	Europe	Sub	1006	T=0.0437	C=0.9563
1000Genomes	South Asian	Sub	978	T=0.083	C=0.917
1000Genomes	American	Sub	694	T=0.081	C=0.919
Genetic variation in the Estonian population	Estonian	Study-wide	4480	T=0.0344	C=0.9656
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	T=0.0330	C=0.9670
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	T=0.0380	C=0.9620
KOREAN population from KRGDB	KOREAN	Study-wide	2930	T=0.1556	C=0.8444
HGDP-CEPH-db Supplement 1	Global	Study-wide	2082	T=0.1114	C=0.8886
HGDP-CEPH-db Supplement 1	Est_Asia	Sub	470	T=0.151	C=0.849
HGDP-CEPH-db Supplement 1	Central_South_Asia	Sub	414	T=0.065	C=0.935
HGDP-CEPH-db Supplement 1	Middle_Est	Sub	350	T=0.103	C=0.897
HGDP-CEPH-db Supplement 1	Europe	Sub	320	T=0.075	C=0.925
HGDP-CEPH-db Supplement 1	Africa	Sub	242	T=0.161	C=0.839
HGDP-CEPH-db Supplement 1	America	Sub	216	T=0.097	C=0.903
HGDP-CEPH-db Supplement 1	Oceania	Sub	70	T=0.20	C=0.80
HapMap	Global	Study-wide	1868	T=0.1017	C=0.8983
HapMap	American	Sub	760	T=0.086	C=0.914
HapMap	African	Sub	686	T=0.089	C=0.911
HapMap	Asian	Sub	250	T=0.204	C=0.796
HapMap	Europe	Sub	172	T=0.076	C=0.924
Korean Genome Project	KOREAN	Study-wide	1832	T=0.1556	C=0.8444
Genome of the Netherlands Release 5	Genome of the Netherlands	Study-wide	998	T=0.030	C=0.970
CNV burdens in cranial meningiomas	Global	Study-wide	788	T=0.122	C=0.878
CNV burdens in cranial meningiomas	CRM	Sub	788	T=0.122	C=0.878
Northern Sweden	ACPOP	Study-wide	600	T=0.017	C=0.983
SGDP_PRJ	Global	Study-wide	546	T=0.097	C=0.903
Qatari	Global	Study-wide	216	T=0.162	C=0.838
A Vietnamese Genetic Variation Database	Global	Study-wide	214	T=0.285	C=0.715
Ancient Sardinia genome-wide 1240k capture data generation and analysis	Global	Study-wide	68	T=0.06	C=0.94
Siberian	Global	Study-wide	56	T=0.04	C=0.96
The Danish reference pan genome	Danish	Study-wide	40	T=0.00	C=1.00

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.147361190T>A
GRCh38.p14 chr 4	NC_000004.12:g.147361190T>C
GRCh37.p13 chr 4	NC_000004.11:g.148282342T>A
GRCh37.p13 chr 4	NC_000004.11:g.148282342T>C

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 4	NC_000004.12:g.147361190=	NC_000004.12:g.147361190T>A	NC_000004.12:g.147361190T>C
GRCh37.p13 chr 4	NC_000004.11:g.148282342=	NC_000004.11:g.148282342T>A	NC_000004.11:g.148282342T>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#.

114 SubSNP, 24 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	TSC-CSHL	ss2237369	Oct 23, 2000 (88)
2	BCM_SSAHASNP	ss10123636	Jul 11, 2003 (116)
3	WI_SSAHASNP	ss11633529	Jul 11, 2003 (116)
4	WI_SSAHASNP	ss14600904	Dec 05, 2003 (119)
5	CSHL-HAPMAP	ss17007817	Feb 27, 2004 (120)
6	SSAHASNP	ss22135731	Apr 05, 2004 (121)
7	PERLEGEN	ss24175741	Sep 20, 2004 (123)
8	AFFY	ss66016428	Dec 01, 2006 (127)
9	AFFY	ss66355173	Dec 01, 2006 (127)
10	ILLUMINA	ss67102286	Dec 01, 2006 (127)
11	ILLUMINA	ss67437818	Dec 01, 2006 (127)
12	ILLUMINA	ss68154675	Dec 12, 2006 (127)
13	ILLUMINA	ss70616965	May 25, 2008 (130)
14	ILLUMINA	ss71165106	May 17, 2007 (127)
15	ILLUMINA	ss75562429	Dec 07, 2007 (129)
16	AFFY	ss76069518	Dec 08, 2007 (130)
17	HGSV	ss78423796	Dec 07, 2007 (129)
18	HGSV	ss79041113	Dec 07, 2007 (129)
19	KRIBB_YJKIM	ss83769446	Dec 15, 2007 (130)
20	BCMHGSC_JDW	ss92821414	Mar 24, 2008 (129)
21	HUMANGENOME_JCVI	ss98872824	Feb 06, 2009 (130)
22	BGI	ss104128201	Dec 01, 2009 (131)
23	1000GENOMES	ss108436495	Jan 23, 2009 (130)
24	1000GENOMES	ss110766769	Jan 25, 2009 (130)
25	ILLUMINA-UK	ss117230650	Feb 14, 2009 (130)
26	ENSEMBL	ss135099895	Dec 01, 2009 (131)
27	ENSEMBL	ss139947981	Dec 01, 2009 (131)
28	ILLUMINA	ss153431449	Dec 01, 2009 (131)
29	GMI	ss158038612	Dec 01, 2009 (131)
30	ILLUMINA	ss159268759	Dec 01, 2009 (131)
31	COMPLETE_GENOMICS	ss162640699	Jul 04, 2010 (132)
32	COMPLETE_GENOMICS	ss164650167	Jul 04, 2010 (132)
33	AFFY	ss172393334	Jul 04, 2010 (132)
34	ILLUMINA	ss172494739	Jul 04, 2010 (132)
35	BUSHMAN	ss199320185	Jul 04, 2010 (132)
36	BCM-HGSC-SUB	ss206257970	Jul 04, 2010 (132)
37	1000GENOMES	ss221277846	Jul 14, 2010 (132)
38	1000GENOMES	ss232646477	Jul 14, 2010 (132)
39	1000GENOMES	ss239883633	Jul 15, 2010 (132)
40	BL	ss253608710	May 09, 2011 (134)
41	GMI	ss277981615	May 04, 2012 (137)
42	GMI	ss285028081	Apr 25, 2013 (138)
43	PJP	ss293221038	May 09, 2011 (134)
44	ILLUMINA	ss536870207	Sep 08, 2015 (146)
45	SSMP	ss651751496	Apr 25, 2013 (138)
46	ILLUMINA	ss832780946	Jul 13, 2019 (153)
47	EVA-GONL	ss980808407	Aug 21, 2014 (142)
48	JMKIDD_LAB	ss1072054386	Aug 21, 2014 (142)
49	1000GENOMES	ss1312307206	Aug 21, 2014 (142)
50	DDI	ss1430091206	Apr 01, 2015 (144)
51	EVA_GENOME_DK	ss1580827762	Apr 01, 2015 (144)
52	EVA_DECODE	ss1590320979	Apr 01, 2015 (144)
53	EVA_UK10K_ALSPAC	ss1611428360	Apr 01, 2015 (144)
54	EVA_UK10K_TWINSUK	ss1654422393	Apr 01, 2015 (144)
55	EVA_SVP	ss1712714293	Apr 01, 2015 (144)
56	HAMMER_LAB	ss1802365509	Sep 08, 2015 (146)
57	WEILL_CORNELL_DGM	ss1924050007	Feb 12, 2016 (147)
58	GENOMED	ss1969901294	Jul 19, 2016 (147)
59	JJLAB	ss2022610973	Sep 14, 2016 (149)
60	USC_VALOUEV	ss2150742646	Dec 20, 2016 (150)
61	HUMAN_LONGEVITY	ss2268142146	Dec 20, 2016 (150)
62	SYSTEMSBIOZJU	ss2625801720	Nov 08, 2017 (151)
63	ILLUMINA	ss2635137767	Nov 08, 2017 (151)
64	GRF	ss2706238215	Nov 08, 2017 (151)
65	GNOMAD	ss2816675386	Nov 08, 2017 (151)
66	SWEGEN	ss2995754901	Nov 08, 2017 (151)
67	ILLUMINA	ss3022424469	Nov 08, 2017 (151)
68	BIOINF_KMB_FNS_UNIBA	ss3025082368	Nov 08, 2017 (151)
69	CSHL	ss3346018710	Nov 08, 2017 (151)
70	ILLUMINA	ss3629088778	Oct 12, 2018 (152)
71	ILLUMINA	ss3638517479	Oct 12, 2018 (152)
72	ILLUMINA	ss3639260879	Oct 12, 2018 (152)
73	ILLUMINA	ss3639928675	Oct 12, 2018 (152)
74	ILLUMINA	ss3643466428	Oct 12, 2018 (152)
75	ILLUMINA	ss3643974622	Oct 12, 2018 (152)
76	URBANLAB	ss3647878563	Oct 12, 2018 (152)
77	ILLUMINA	ss3652914617	Oct 12, 2018 (152)
78	EGCUT_WGS	ss3663660800	Jul 13, 2019 (153)
79	EVA_DECODE	ss3713297458	Jul 13, 2019 (153)
80	ILLUMINA	ss3726179101	Jul 13, 2019 (153)
81	ACPOP	ss3731714357	Jul 13, 2019 (153)
82	EVA	ss3762559912	Jul 13, 2019 (153)
83	PACBIO	ss3784896504	Jul 13, 2019 (153)
84	PACBIO	ss3790327801	Jul 13, 2019 (153)
85	PACBIO	ss3795203354	Jul 13, 2019 (153)
86	KHV_HUMAN_GENOMES	ss3805721288	Jul 13, 2019 (153)
87	EVA	ss3828870587	Apr 26, 2020 (154)
88	EVA	ss3837885837	Apr 26, 2020 (154)
89	EVA	ss3843325969	Apr 26, 2020 (154)
90	HGDP	ss3847768194	Apr 26, 2020 (154)
91	SGDP_PRJ	ss3860315810	Apr 26, 2020 (154)
92	KRGDB	ss3906654285	Apr 26, 2020 (154)
93	KOGIC	ss3955351110	Apr 26, 2020 (154)
94	EVA	ss3984536604	Apr 26, 2021 (155)
95	EVA	ss3985101654	Apr 26, 2021 (155)
96	TOPMED	ss4636311137	Apr 26, 2021 (155)
97	TOMMO_GENOMICS	ss5168560429	Apr 26, 2021 (155)
98	1000G_HIGH_COVERAGE	ss5261452598	Oct 13, 2022 (156)
99	GENOGRAPHIC	ss5314501762	Oct 13, 2022 (156)
100	EVA	ss5353082012	Oct 13, 2022 (156)
101	HUGCELL_USP	ss5459960732	Oct 13, 2022 (156)
102	EVA	ss5507777186	Oct 13, 2022 (156)
103	1000G_HIGH_COVERAGE	ss5543777553	Oct 13, 2022 (156)
104	SANFORD_IMAGENETICS	ss5624570350	Oct 13, 2022 (156)
105	SANFORD_IMAGENETICS	ss5636347480	Oct 13, 2022 (156)
106	TOMMO_GENOMICS	ss5703705317	Oct 13, 2022 (156)
107	YY_MCH	ss5805644527	Oct 13, 2022 (156)
108	EVA	ss5844882345	Oct 13, 2022 (156)
109	EVA	ss5847252874	Oct 13, 2022 (156)
110	EVA	ss5848027974	Oct 13, 2022 (156)
111	EVA	ss5854496633	Oct 13, 2022 (156)
112	EVA	ss5865992610	Oct 13, 2022 (156)
113	EVA	ss5964750633	Oct 13, 2022 (156)
114	EVA	ss5979717816	Oct 13, 2022 (156)
115	1000Genomes	NC_000004.11 - 148282342	Oct 12, 2018 (152)
116	1000Genomes_30x	NC_000004.12 - 147361190	Oct 13, 2022 (156)
117	The Avon Longitudinal Study of Parents and Children	NC_000004.11 - 148282342	Oct 12, 2018 (152)
118	Genetic variation in the Estonian population	NC_000004.11 - 148282342	Oct 12, 2018 (152)
119	Genographic Project	NC_000004.12 - 147361190	Oct 13, 2022 (156)
120	The Danish reference pan genome	NC_000004.11 - 148282342	Apr 26, 2020 (154)
121	gnomAD - Genomes	NC_000004.12 - 147361190	Apr 26, 2021 (155)
122	Genome of the Netherlands Release 5	NC_000004.11 - 148282342	Apr 26, 2020 (154)
123	HGDP-CEPH-db Supplement 1	NC_000004.10 - 148501792	Apr 26, 2020 (154)
124	HapMap	NC_000004.12 - 147361190	Apr 26, 2020 (154)
125	KOREAN population from KRGDB	NC_000004.11 - 148282342	Apr 26, 2020 (154)
126	Korean Genome Project	NC_000004.12 - 147361190	Apr 26, 2020 (154)
127	Northern Sweden	NC_000004.11 - 148282342	Jul 13, 2019 (153)
128	Ancient Sardinia genome-wide 1240k capture data generation and analysis	NC_000004.11 - 148282342	Apr 26, 2021 (155)
129	CNV burdens in cranial meningiomas	NC_000004.11 - 148282342	Apr 26, 2021 (155)
130	Qatari	NC_000004.11 - 148282342	Apr 26, 2020 (154)
131	SGDP_PRJ	NC_000004.11 - 148282342	Apr 26, 2020 (154)
132	Siberian	NC_000004.11 - 148282342	Apr 26, 2020 (154)
133	8.3KJPN	NC_000004.11 - 148282342	Apr 26, 2021 (155)
134	14KJPN	NC_000004.12 - 147361190	Oct 13, 2022 (156)
135	TopMed	NC_000004.12 - 147361190	Apr 26, 2021 (155)
136	UK 10K study - Twins	NC_000004.11 - 148282342	Oct 12, 2018 (152)
137	A Vietnamese Genetic Variation Database	NC_000004.11 - 148282342	Jul 13, 2019 (153)
138	ALFA	NC_000004.12 - 147361190	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)
rs17658156	Oct 07, 2004 (123)
rs56579538	May 25, 2008 (130)
rs60258280	May 25, 2008 (130)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
80088, 11965391783, ss5314501762	NC_000004.12:147361189:T:A	NC_000004.12:147361189:T:A	(self)
ss78423796, ss79041113, ss3639260879, ss3639928675, ss3643974622	NC_000004.9:148639946:T:C	NC_000004.12:147361189:T:C	(self)
446086, ss66355173, ss76069518, ss92821414, ss108436495, ss110766769, ss117230650, ss162640699, ss164650167, ss172393334, ss199320185, ss206257970, ss253608710, ss277981615, ss285028081, ss293221038, ss1590320979, ss1712714293, ss2635137767, ss3643466428, ss3847768194	NC_000004.10:148501791:T:C	NC_000004.12:147361189:T:C	(self)
23800919, 13233156, 9399048, 6992701, 5862956, 13831679, 4999222, 327581, 85966, 6091937, 12332790, 3259000, 26529736, 13233156, 2919384, ss221277846, ss232646477, ss239883633, ss536870207, ss651751496, ss832780946, ss980808407, ss1072054386, ss1312307206, ss1430091206, ss1580827762, ss1611428360, ss1654422393, ss1802365509, ss1924050007, ss1969901294, ss2022610973, ss2150742646, ss2625801720, ss2706238215, ss2816675386, ss2995754901, ss3022424469, ss3346018710, ss3629088778, ss3638517479, ss3652914617, ss3663660800, ss3731714357, ss3762559912, ss3784896504, ss3790327801, ss3795203354, ss3828870587, ss3837885837, ss3860315810, ss3906654285, ss3984536604, ss3985101654, ss5168560429, ss5353082012, ss5507777186, ss5624570350, ss5636347480, ss5844882345, ss5847252874, ss5848027974, ss5964750633, ss5979717816	NC_000004.11:148282341:T:C	NC_000004.12:147361189:T:C	(self)
31303488, 80088, 168582154, 2730968, 11729111, 37542421, 473688693, 11965391783, ss2268142146, ss3025082368, ss3647878563, ss3713297458, ss3726179101, ss3805721288, ss3843325969, ss3955351110, ss4636311137, ss5261452598, ss5314501762, ss5459960732, ss5543777553, ss5703705317, ss5805644527, ss5854496633, ss5865992610	NC_000004.12:147361189:T:C	NC_000004.12:147361189:T:C	(self)
ss2237369, ss24175741, ss66016428, ss67102286, ss67437818, ss68154675, ss70616965, ss71165106, ss75562429, ss83769446, ss98872824, ss104128201, ss135099895, ss139947981, ss153431449, ss158038612, ss159268759, ss172494739	NT_016354.19:72830062:T:C	NC_000004.12:147361189:T:C	(self)
ss10123636, ss11633529	NT_016606.15:9802006:T:C	NC_000004.12:147361189:T:C	(self)
ss14600904, ss17007817, ss22135731	NT_016606.16:9830397:T:C	NC_000004.12:147361189: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 rs1429138

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

rs1429138