Name: rs4657642
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.

rs4657642

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr1:167168712 (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>G
Variation Type: SNV Single Nucleotide Variation
Frequency: G=0.315751 (83576/264690, TOPMED)
G=0.191022 (39174/205076, GENOGRAPHIC)
G=0.176612 (34291/194160, ALFA) (+ 20 more)
G=0.308094 (43151/140058, GnomAD)
T=0.48871 (13809/28256, 14KJPN)
T=0.48896 (8195/16760, 8.3KJPN)
G=0.4136 (2649/6404, 1000G_30x)
G=0.4115 (2061/5008, 1000G)
G=0.1540 (690/4480, Estonian)
G=0.1759 (678/3854, ALSPAC)
G=0.1694 (628/3708, TWINSUK)
T=0.4191 (1228/2930, KOREAN)
G=0.3484 (726/2084, HGDP_Stanford)
G=0.4651 (879/1890, HapMap)
T=0.4132 (757/1832, Korea1K)
G=0.161 (161/998, GoNL)
G=0.213 (128/600, NorthernSweden)
T=0.318 (98/308, SGDP_PRJ)
G=0.319 (69/216, Qatari)
T=0.346 (74/214, Vietnamese)
G=0.04 (4/92, Ancient Sardinia)
G=0.07 (3/40, GENOME_DK)
T=0.47 (14/30, Siberian)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: LOC105371601 : 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	194160	T=0.823388	A=0.000000, G=0.176612
European	Sub	169478	T=0.838687	A=0.000000, G=0.161313
African	Sub	5150	T=0.4336	A=0.0000, G=0.5664
African Others	Sub	188	T=0.335	A=0.000, G=0.665
African American	Sub	4962	T=0.4373	A=0.0000, G=0.5627
Asian	Sub	604	T=0.435	A=0.000, G=0.565
East Asian	Sub	476	T=0.450	A=0.000, G=0.550
Other Asian	Sub	128	T=0.383	A=0.000, G=0.617
Latin American 1	Sub	780	T=0.765	A=0.000, G=0.235
Latin American 2	Sub	6742	T=0.8708	A=0.0000, G=0.1292
South Asian	Sub	4996	T=0.7498	A=0.0000, G=0.2502
Other	Sub	6410	T=0.7832	A=0.0000, G=0.2168

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=0.684249	G=0.315751
Genographic Project	Global	Study-wide	205076	T=0.808978	G=0.191022
Allele Frequency Aggregator	Total	Global	194160	T=0.823388	A=0.000000, G=0.176612
Allele Frequency Aggregator	European	Sub	169478	T=0.838687	A=0.000000, G=0.161313
Allele Frequency Aggregator	Latin American 2	Sub	6742	T=0.8708	A=0.0000, G=0.1292
Allele Frequency Aggregator	Other	Sub	6410	T=0.7832	A=0.0000, G=0.2168
Allele Frequency Aggregator	African	Sub	5150	T=0.4336	A=0.0000, G=0.5664
Allele Frequency Aggregator	South Asian	Sub	4996	T=0.7498	A=0.0000, G=0.2502
Allele Frequency Aggregator	Latin American 1	Sub	780	T=0.765	A=0.000, G=0.235
Allele Frequency Aggregator	Asian	Sub	604	T=0.435	A=0.000, G=0.565
gnomAD - Genomes	Global	Study-wide	140058	T=0.691906	G=0.308094
gnomAD - Genomes	European	Sub	75886	T=0.82605	G=0.17395
gnomAD - Genomes	African	Sub	41932	T=0.41384	G=0.58616
gnomAD - Genomes	American	Sub	13642	T=0.83419	G=0.16581
gnomAD - Genomes	Ashkenazi Jewish	Sub	3320	T=0.8479	G=0.1521
gnomAD - Genomes	East Asian	Sub	3128	T=0.3504	G=0.6496
gnomAD - Genomes	Other	Sub	2150	T=0.7335	G=0.2665
14KJPN	JAPANESE	Study-wide	28256	T=0.48871	G=0.51129
8.3KJPN	JAPANESE	Study-wide	16760	T=0.48896	G=0.51104
1000Genomes_30x	Global	Study-wide	6404	T=0.5864	G=0.4136
1000Genomes_30x	African	Sub	1786	T=0.3561	G=0.6439
1000Genomes_30x	Europe	Sub	1266	T=0.8254	G=0.1746
1000Genomes_30x	South Asian	Sub	1202	T=0.7180	G=0.2820
1000Genomes_30x	East Asian	Sub	1170	T=0.3359	G=0.6641
1000Genomes_30x	American	Sub	980	T=0.835	G=0.165
1000Genomes	Global	Study-wide	5008	T=0.5885	G=0.4115
1000Genomes	African	Sub	1322	T=0.3638	G=0.6362
1000Genomes	East Asian	Sub	1008	T=0.3433	G=0.6567
1000Genomes	Europe	Sub	1006	T=0.8201	G=0.1799
1000Genomes	South Asian	Sub	978	T=0.728	G=0.272
1000Genomes	American	Sub	694	T=0.840	G=0.160
Genetic variation in the Estonian population	Estonian	Study-wide	4480	T=0.8460	G=0.1540
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	T=0.8241	G=0.1759
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	T=0.8306	G=0.1694
KOREAN population from KRGDB	KOREAN	Study-wide	2930	T=0.4191	G=0.5809
HGDP-CEPH-db Supplement 1	Global	Study-wide	2084	T=0.6516	G=0.3484
HGDP-CEPH-db Supplement 1	Est_Asia	Sub	470	T=0.436	G=0.564
HGDP-CEPH-db Supplement 1	Central_South_Asia	Sub	414	T=0.737	G=0.263
HGDP-CEPH-db Supplement 1	Middle_Est	Sub	350	T=0.760	G=0.240
HGDP-CEPH-db Supplement 1	Europe	Sub	320	T=0.825	G=0.175
HGDP-CEPH-db Supplement 1	Africa	Sub	242	T=0.314	G=0.686
HGDP-CEPH-db Supplement 1	America	Sub	216	T=0.935	G=0.065
HGDP-CEPH-db Supplement 1	Oceania	Sub	72	T=0.56	G=0.44
HapMap	Global	Study-wide	1890	T=0.5349	G=0.4651
HapMap	American	Sub	770	T=0.670	G=0.330
HapMap	African	Sub	692	T=0.355	G=0.645
HapMap	Asian	Sub	252	T=0.389	G=0.611
HapMap	Europe	Sub	176	T=0.858	G=0.142
Korean Genome Project	KOREAN	Study-wide	1832	T=0.4132	G=0.5868
Genome of the Netherlands Release 5	Genome of the Netherlands	Study-wide	998	T=0.839	G=0.161
Northern Sweden	ACPOP	Study-wide	600	T=0.787	G=0.213
SGDP_PRJ	Global	Study-wide	308	T=0.318	G=0.682
Qatari	Global	Study-wide	216	T=0.681	G=0.319
A Vietnamese Genetic Variation Database	Global	Study-wide	214	T=0.346	G=0.654
Ancient Sardinia genome-wide 1240k capture data generation and analysis	Global	Study-wide	92	T=0.96	G=0.04
The Danish reference pan genome	Danish	Study-wide	40	T=0.93	G=0.07
Siberian	Global	Study-wide	30	T=0.47	G=0.53

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.167168712T>A
GRCh38.p14 chr 1	NC_000001.11:g.167168712T>G
GRCh37.p13 chr 1	NC_000001.10:g.167137949T>A
GRCh37.p13 chr 1	NC_000001.10:g.167137949T>G

Gene: LOC105371601, uncharacterized LOC105371601 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
LOC105371601 transcript	XR_922250.3:n.	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	G
GRCh38.p14 chr 1	NC_000001.11:g.167168712=	NC_000001.11:g.167168712T>A	NC_000001.11:g.167168712T>G
GRCh37.p13 chr 1	NC_000001.10:g.167137949=	NC_000001.10:g.167137949T>A	NC_000001.10:g.167137949T>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#.

115 SubSNP, 23 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	WI_SSAHASNP	ss6411131	Feb 20, 2003 (111)
2	PERLEGEN	ss23145063	Sep 20, 2004 (123)
3	ILLUMINA	ss67354125	Dec 01, 2006 (127)
4	ILLUMINA	ss67744004	Dec 01, 2006 (127)
5	ILLUMINA	ss68232514	Dec 12, 2006 (127)
6	PERLEGEN	ss68783609	May 17, 2007 (127)
7	ILLUMINA	ss70813596	May 25, 2008 (130)
8	ILLUMINA	ss71394179	May 17, 2007 (127)
9	ILLUMINA	ss75591561	Dec 07, 2007 (129)
10	HGSV	ss81215175	Dec 15, 2007 (130)
11	HGSV	ss81896749	Dec 15, 2007 (130)
12	KRIBB_YJKIM	ss84306596	Dec 15, 2007 (130)
13	HGSV	ss84377616	Dec 15, 2007 (130)
14	BCMHGSC_JDW	ss87857424	Mar 23, 2008 (129)
15	1000GENOMES	ss108672612	Jan 23, 2009 (130)
16	1000GENOMES	ss111292266	Jan 25, 2009 (130)
17	ILLUMINA-UK	ss119074264	Feb 15, 2009 (130)
18	ENSEMBL	ss138098542	Dec 01, 2009 (131)
19	ILLUMINA	ss154305034	Dec 01, 2009 (131)
20	GMI	ss155884227	Dec 01, 2009 (131)
21	ILLUMINA	ss159481844	Dec 01, 2009 (131)
22	ILLUMINA	ss160694756	Dec 01, 2009 (131)
23	COMPLETE_GENOMICS	ss164336154	Jul 04, 2010 (132)
24	COMPLETE_GENOMICS	ss167240016	Jul 04, 2010 (132)
25	ILLUMINA	ss173770404	Jul 04, 2010 (132)
26	BUSHMAN	ss199198608	Jul 04, 2010 (132)
27	BCM-HGSC-SUB	ss205424420	Jul 04, 2010 (132)
28	1000GENOMES	ss218698161	Jul 14, 2010 (132)
29	1000GENOMES	ss230767056	Jul 14, 2010 (132)
30	1000GENOMES	ss238408296	Jul 15, 2010 (132)
31	GMI	ss276088389	May 04, 2012 (137)
32	GMI	ss284169075	Apr 25, 2013 (138)
33	PJP	ss290656247	May 09, 2011 (134)
34	ILLUMINA	ss480991919	May 04, 2012 (137)
35	ILLUMINA	ss481012484	May 04, 2012 (137)
36	ILLUMINA	ss481993142	Sep 08, 2015 (146)
37	ILLUMINA	ss485290846	May 04, 2012 (137)
38	ILLUMINA	ss537254044	Sep 08, 2015 (146)
39	TISHKOFF	ss554807966	Apr 25, 2013 (138)
40	SSMP	ss648475452	Apr 25, 2013 (138)
41	ILLUMINA	ss778913243	Aug 21, 2014 (142)
42	ILLUMINA	ss783091313	Aug 21, 2014 (142)
43	ILLUMINA	ss784048711	Aug 21, 2014 (142)
44	ILLUMINA	ss832349786	Apr 01, 2015 (144)
45	ILLUMINA	ss832993271	Aug 21, 2014 (142)
46	ILLUMINA	ss833584100	Aug 21, 2014 (142)
47	ILLUMINA	ss834374614	Aug 21, 2014 (142)
48	EVA-GONL	ss975776337	Aug 21, 2014 (142)
49	JMKIDD_LAB	ss1068337138	Aug 21, 2014 (142)
50	1000GENOMES	ss1293281299	Aug 21, 2014 (142)
51	DDI	ss1426006451	Apr 01, 2015 (144)
52	EVA_GENOME_DK	ss1574452537	Apr 01, 2015 (144)
53	EVA_DECODE	ss1585161267	Apr 01, 2015 (144)
54	EVA_UK10K_ALSPAC	ss1601403163	Apr 01, 2015 (144)
55	EVA_UK10K_TWINSUK	ss1644397196	Apr 01, 2015 (144)
56	EVA_SVP	ss1712378612	Apr 01, 2015 (144)
57	ILLUMINA	ss1751879365	Sep 08, 2015 (146)
58	HAMMER_LAB	ss1795217909	Sep 08, 2015 (146)
59	WEILL_CORNELL_DGM	ss1919012579	Feb 12, 2016 (147)
60	JJLAB	ss2020021869	Sep 14, 2016 (149)
61	USC_VALOUEV	ss2148049106	Dec 20, 2016 (150)
62	HUMAN_LONGEVITY	ss2167250775	Dec 20, 2016 (150)
63	SYSTEMSBIOZJU	ss2624520573	Nov 08, 2017 (151)
64	ILLUMINA	ss2632588207	Nov 08, 2017 (151)
65	GRF	ss2698026535	Nov 08, 2017 (151)
66	GNOMAD	ss2762317392	Nov 08, 2017 (151)
67	SWEGEN	ss2987896338	Nov 08, 2017 (151)
68	BIOINF_KMB_FNS_UNIBA	ss3023768873	Nov 08, 2017 (151)
69	CSHL	ss3343752769	Nov 08, 2017 (151)
70	ILLUMINA	ss3626231751	Oct 11, 2018 (152)
71	ILLUMINA	ss3630620315	Oct 11, 2018 (152)
72	ILLUMINA	ss3632913740	Oct 11, 2018 (152)
73	ILLUMINA	ss3633609254	Oct 11, 2018 (152)
74	ILLUMINA	ss3634356360	Oct 11, 2018 (152)
75	ILLUMINA	ss3635302624	Oct 11, 2018 (152)
76	ILLUMINA	ss3636035304	Oct 11, 2018 (152)
77	ILLUMINA	ss3637053123	Oct 11, 2018 (152)
78	ILLUMINA	ss3637793440	Oct 11, 2018 (152)
79	ILLUMINA	ss3638913322	Oct 11, 2018 (152)
80	ILLUMINA	ss3639768711	Oct 11, 2018 (152)
81	ILLUMINA	ss3640063714	Oct 11, 2018 (152)
82	ILLUMINA	ss3642802120	Oct 11, 2018 (152)
83	ILLUMINA	ss3643822048	Oct 11, 2018 (152)
84	EGCUT_WGS	ss3655839305	Jul 12, 2019 (153)
85	EVA_DECODE	ss3687956482	Jul 12, 2019 (153)
86	ACPOP	ss3727564118	Jul 12, 2019 (153)
87	ILLUMINA	ss3744657243	Jul 12, 2019 (153)
88	EVA	ss3746917623	Jul 12, 2019 (153)
89	ILLUMINA	ss3772158303	Jul 12, 2019 (153)
90	KHV_HUMAN_GENOMES	ss3799918327	Jul 12, 2019 (153)
91	EVA	ss3826471388	Apr 25, 2020 (154)
92	EVA	ss3836631834	Apr 25, 2020 (154)
93	EVA	ss3842041677	Apr 25, 2020 (154)
94	HGDP	ss3847352737	Apr 25, 2020 (154)
95	SGDP_PRJ	ss3850189677	Apr 25, 2020 (154)
96	KRGDB	ss3895422176	Apr 25, 2020 (154)
97	KOGIC	ss3945830742	Apr 25, 2020 (154)
98	EVA	ss3984831615	Apr 25, 2021 (155)
99	EVA	ss4016943465	Apr 25, 2021 (155)
100	TOPMED	ss4471401410	Apr 25, 2021 (155)
101	TOMMO_GENOMICS	ss5146886005	Apr 25, 2021 (155)
102	1000G_HIGH_COVERAGE	ss5244600882	Oct 12, 2022 (156)
103	GENOGRAPHIC	ss5314468698	Oct 12, 2022 (156)
104	EVA	ss5314658245	Oct 12, 2022 (156)
105	EVA	ss5322612081	Oct 12, 2022 (156)
106	HUGCELL_USP	ss5445153873	Oct 12, 2022 (156)
107	1000G_HIGH_COVERAGE	ss5518083842	Oct 12, 2022 (156)
108	SANFORD_IMAGENETICS	ss5626767439	Oct 12, 2022 (156)
109	TOMMO_GENOMICS	ss5674201177	Oct 12, 2022 (156)
110	EVA	ss5799501908	Oct 12, 2022 (156)
111	YY_MCH	ss5801338775	Oct 12, 2022 (156)
112	EVA	ss5832788052	Oct 12, 2022 (156)
113	EVA	ss5849145822	Oct 12, 2022 (156)
114	EVA	ss5910597212	Oct 12, 2022 (156)
115	EVA	ss5938567509	Oct 12, 2022 (156)
116	1000Genomes	NC_000001.10 - 167137949	Oct 11, 2018 (152)
117	1000Genomes_30x	NC_000001.11 - 167168712	Oct 12, 2022 (156)
118	The Avon Longitudinal Study of Parents and Children	NC_000001.10 - 167137949	Oct 11, 2018 (152)
119	Genetic variation in the Estonian population	NC_000001.10 - 167137949	Oct 11, 2018 (152)
120	Genographic Project	NC_000001.11 - 167168712	Oct 12, 2022 (156)
121	The Danish reference pan genome	NC_000001.10 - 167137949	Apr 25, 2020 (154)
122	gnomAD - Genomes	NC_000001.11 - 167168712	Apr 25, 2021 (155)
123	Genome of the Netherlands Release 5	NC_000001.10 - 167137949	Apr 25, 2020 (154)
124	HGDP-CEPH-db Supplement 1	NC_000001.9 - 165404573	Apr 25, 2020 (154)
125	HapMap	NC_000001.11 - 167168712	Apr 25, 2020 (154)
126	KOREAN population from KRGDB	NC_000001.10 - 167137949	Apr 25, 2020 (154)
127	Korean Genome Project	NC_000001.11 - 167168712	Apr 25, 2020 (154)
128	Northern Sweden	NC_000001.10 - 167137949	Jul 12, 2019 (153)
129	Ancient Sardinia genome-wide 1240k capture data generation and analysis	NC_000001.10 - 167137949	Apr 25, 2021 (155)
130	Qatari	NC_000001.10 - 167137949	Apr 25, 2020 (154)
131	SGDP_PRJ	NC_000001.10 - 167137949	Apr 25, 2020 (154)
132	Siberian	NC_000001.10 - 167137949	Apr 25, 2020 (154)
133	8.3KJPN	NC_000001.10 - 167137949	Apr 25, 2021 (155)
134	14KJPN	NC_000001.11 - 167168712	Oct 12, 2022 (156)
135	TopMed	NC_000001.11 - 167168712	Apr 25, 2021 (155)
136	UK 10K study - Twins	NC_000001.10 - 167137949	Oct 11, 2018 (152)
137	A Vietnamese Genetic Variation Database	NC_000001.10 - 167137949	Jul 12, 2019 (153)
138	ALFA	NC_000001.11 - 167168712	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)
rs59581355	May 25, 2008 (130)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
15152808383	NC_000001.11:167168711:T:A	NC_000001.11:167168711:T:A	(self)
ss81215175, ss81896749, ss84377616, ss3638913322, ss3639768711, ss3643822048	NC_000001.8:163869606:T:G	NC_000001.11:167168711:T:G	(self)
30629, ss87857424, ss108672612, ss111292266, ss119074264, ss160694756, ss164336154, ss167240016, ss199198608, ss205424420, ss276088389, ss284169075, ss290656247, ss480991919, ss1585161267, ss1712378612, ss3642802120, ss3847352737	NC_000001.9:165404572:T:G	NC_000001.11:167168711:T:G	(self)
4085214, 2228406, 1577553, 1745226, 969102, 2599570, 848983, 57542, 1054509, 2206657, 565460, 4855312, 2228406, 479238, ss218698161, ss230767056, ss238408296, ss481012484, ss481993142, ss485290846, ss537254044, ss554807966, ss648475452, ss778913243, ss783091313, ss784048711, ss832349786, ss832993271, ss833584100, ss834374614, ss975776337, ss1068337138, ss1293281299, ss1426006451, ss1574452537, ss1601403163, ss1644397196, ss1751879365, ss1795217909, ss1919012579, ss2020021869, ss2148049106, ss2624520573, ss2632588207, ss2698026535, ss2762317392, ss2987896338, ss3343752769, ss3626231751, ss3630620315, ss3632913740, ss3633609254, ss3634356360, ss3635302624, ss3636035304, ss3637053123, ss3637793440, ss3640063714, ss3655839305, ss3727564118, ss3744657243, ss3746917623, ss3772158303, ss3826471388, ss3836631834, ss3850189677, ss3895422176, ss3984831615, ss4016943465, ss5146886005, ss5314658245, ss5322612081, ss5626767439, ss5799501908, ss5832788052, ss5938567509	NC_000001.10:167137948:T:G	NC_000001.11:167168711:T:G	(self)
5609777, 35622, 29596928, 196149, 2208743, 8038281, 35007745, 15152808383, ss2167250775, ss3023768873, ss3687956482, ss3799918327, ss3842041677, ss3945830742, ss4471401410, ss5244600882, ss5314468698, ss5445153873, ss5518083842, ss5674201177, ss5801338775, ss5849145822, ss5910597212	NC_000001.11:167168711:T:G	NC_000001.11:167168711:T:G	(self)
ss6411131, ss23145063, ss67354125, ss67744004, ss68232514, ss68783609, ss70813596, ss71394179, ss75591561, ss84306596, ss138098542, ss154305034, ss155884227, ss159481844, ss173770404	NT_004487.19:18626590:T:G	NC_000001.11:167168711: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 rs4657642

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

rs4657642