Name: rs953741
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.

rs953741

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr5:178902845 (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>C
Variation Type: SNV Single Nucleotide Variation
Frequency: C=0.219581 (58121/264690, TOPMED)
C=0.299250 (61369/205076, GENOGRAPHIC)
C=0.298742 (60359/202044, ALFA) (+ 21 more)
C=0.243134 (34049/140042, GnomAD)
C=0.03089 (873/28258, 14KJPN)
C=0.03264 (547/16760, 8.3KJPN)
C=0.1494 (957/6404, 1000G_30x)
C=0.1488 (745/5008, 1000G)
C=0.3549 (1590/4480, Estonian)
C=0.3199 (1233/3854, ALSPAC)
C=0.3247 (1204/3708, TWINSUK)
C=0.0329 (96/2922, KOREAN)
C=0.1550 (323/2084, HGDP_Stanford)
C=0.1279 (242/1892, HapMap)
C=0.2745 (303/1104, Daghestan)
C=0.339 (338/998, GoNL)
C=0.052 (41/790, PRJEB37584)
C=0.313 (188/600, NorthernSweden)
C=0.218 (47/216, Qatari)
C=0.028 (6/216, Vietnamese)
T=0.392 (47/120, SGDP_PRJ)
C=0.30 (12/40, GENOME_DK)
T=0.50 (11/22, Siberian)
C=0.50 (11/22, Siberian)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: ZFP2 : Intron Variant
Publications: 2 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	202044	T=0.701258	C=0.298742
European	Sub	174826	T=0.685316	C=0.314684
African	Sub	7092	T=0.8995	C=0.1005
African Others	Sub	264	T=0.932	C=0.068
African American	Sub	6828	T=0.8982	C=0.1018
Asian	Sub	702	T=0.960	C=0.040
East Asian	Sub	556	T=0.957	C=0.043
Other Asian	Sub	146	T=0.973	C=0.027
Latin American 1	Sub	842	T=0.772	C=0.228
Latin American 2	Sub	6860	T=0.7867	C=0.2133
South Asian	Sub	5040	T=0.7704	C=0.2296
Other	Sub	6682	T=0.7320	C=0.2680

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=0.780419	C=0.219581
Genographic Project	Global	Study-wide	205076	T=0.700750	C=0.299250
Allele Frequency Aggregator	Total	Global	202044	T=0.701258	C=0.298742
Allele Frequency Aggregator	European	Sub	174826	T=0.685316	C=0.314684
Allele Frequency Aggregator	African	Sub	7092	T=0.8995	C=0.1005
Allele Frequency Aggregator	Latin American 2	Sub	6860	T=0.7867	C=0.2133
Allele Frequency Aggregator	Other	Sub	6682	T=0.7320	C=0.2680
Allele Frequency Aggregator	South Asian	Sub	5040	T=0.7704	C=0.2296
Allele Frequency Aggregator	Latin American 1	Sub	842	T=0.772	C=0.228
Allele Frequency Aggregator	Asian	Sub	702	T=0.960	C=0.040
gnomAD - Genomes	Global	Study-wide	140042	T=0.756866	C=0.243134
gnomAD - Genomes	European	Sub	75798	T=0.66632	C=0.33368
gnomAD - Genomes	African	Sub	41996	T=0.90090	C=0.09910
gnomAD - Genomes	American	Sub	13642	T=0.77408	C=0.22592
gnomAD - Genomes	Ashkenazi Jewish	Sub	3322	T=0.7294	C=0.2706
gnomAD - Genomes	East Asian	Sub	3134	T=0.9614	C=0.0386
gnomAD - Genomes	Other	Sub	2150	T=0.7707	C=0.2293
14KJPN	JAPANESE	Study-wide	28258	T=0.96911	C=0.03089
8.3KJPN	JAPANESE	Study-wide	16760	T=0.96736	C=0.03264
1000Genomes_30x	Global	Study-wide	6404	T=0.8506	C=0.1494
1000Genomes_30x	African	Sub	1786	T=0.9479	C=0.0521
1000Genomes_30x	Europe	Sub	1266	T=0.6643	C=0.3357
1000Genomes_30x	South Asian	Sub	1202	T=0.8178	C=0.1822
1000Genomes_30x	East Asian	Sub	1170	T=0.9607	C=0.0393
1000Genomes_30x	American	Sub	980	T=0.822	C=0.178
1000Genomes	Global	Study-wide	5008	T=0.8512	C=0.1488
1000Genomes	African	Sub	1322	T=0.9440	C=0.0560
1000Genomes	East Asian	Sub	1008	T=0.9593	C=0.0407
1000Genomes	Europe	Sub	1006	T=0.6640	C=0.3360
1000Genomes	South Asian	Sub	978	T=0.816	C=0.184
1000Genomes	American	Sub	694	T=0.839	C=0.161
Genetic variation in the Estonian population	Estonian	Study-wide	4480	T=0.6451	C=0.3549
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	T=0.6801	C=0.3199
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	T=0.6753	C=0.3247
KOREAN population from KRGDB	KOREAN	Study-wide	2922	T=0.9671	C=0.0329
HGDP-CEPH-db Supplement 1	Global	Study-wide	2084	T=0.8450	C=0.1550
HGDP-CEPH-db Supplement 1	Est_Asia	Sub	470	T=0.943	C=0.057
HGDP-CEPH-db Supplement 1	Central_South_Asia	Sub	414	T=0.797	C=0.203
HGDP-CEPH-db Supplement 1	Middle_Est	Sub	350	T=0.760	C=0.240
HGDP-CEPH-db Supplement 1	Europe	Sub	320	T=0.703	C=0.297
HGDP-CEPH-db Supplement 1	Africa	Sub	242	T=0.946	C=0.054
HGDP-CEPH-db Supplement 1	America	Sub	216	T=0.907	C=0.093
HGDP-CEPH-db Supplement 1	Oceania	Sub	72	T=1.00	C=0.00
HapMap	Global	Study-wide	1892	T=0.8721	C=0.1279
HapMap	American	Sub	770	T=0.795	C=0.205
HapMap	African	Sub	692	T=0.952	C=0.048
HapMap	Asian	Sub	254	T=0.976	C=0.024
HapMap	Europe	Sub	176	T=0.744	C=0.256
Genome-wide autozygosity in Daghestan	Global	Study-wide	1104	T=0.7255	C=0.2745
Genome-wide autozygosity in Daghestan	Daghestan	Sub	618	T=0.693	C=0.307
Genome-wide autozygosity in Daghestan	Near_East	Sub	142	T=0.739	C=0.261
Genome-wide autozygosity in Daghestan	Central Asia	Sub	116	T=0.793	C=0.207
Genome-wide autozygosity in Daghestan	Europe	Sub	106	T=0.670	C=0.330
Genome-wide autozygosity in Daghestan	South Asian	Sub	86	T=0.92	C=0.08
Genome-wide autozygosity in Daghestan	Caucasus	Sub	36	T=0.72	C=0.28
Genome of the Netherlands Release 5	Genome of the Netherlands	Study-wide	998	T=0.661	C=0.339
CNV burdens in cranial meningiomas	Global	Study-wide	790	T=0.948	C=0.052
CNV burdens in cranial meningiomas	CRM	Sub	790	T=0.948	C=0.052
Northern Sweden	ACPOP	Study-wide	600	T=0.687	C=0.313
Qatari	Global	Study-wide	216	T=0.782	C=0.218
A Vietnamese Genetic Variation Database	Global	Study-wide	216	T=0.972	C=0.028
SGDP_PRJ	Global	Study-wide	120	T=0.392	C=0.608
The Danish reference pan genome	Danish	Study-wide	40	T=0.70	C=0.30
Siberian	Global	Study-wide	22	T=0.50	C=0.50

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 5	NC_000005.10:g.178902845T>C
GRCh37.p13 chr 5	NC_000005.9:g.178329846T>C

Gene: ZFP2, ZFP2 zinc finger protein (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
ZFP2 transcript	NM_030613.4:c.-450+6871T>C	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=	C
GRCh38.p14 chr 5	NC_000005.10:g.178902845=	NC_000005.10:g.178902845T>C
GRCh37.p13 chr 5	NC_000005.9:g.178329846=	NC_000005.9:g.178329846T>C
ZFP2 transcript	NM_030613.2:c.-450+6871=	NM_030613.2:c.-450+6871T>C
ZFP2 transcript	NM_030613.4:c.-450+6871=	NM_030613.4:c.-450+6871T>C
ZFP2 transcript variant X3	XM_005265991.1:c.-453+6871=	XM_005265991.1:c.-453+6871T>C
ZFP2 transcript variant X4	XM_005265992.1:c.-78+6871=	XM_005265992.1:c.-78+6871T>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#.

111 SubSNP, 23 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	TSC-CSHL	ss1398209	Oct 05, 2000 (86)
2	CSHL-HAPMAP	ss17051124	Feb 27, 2004 (120)
3	PERLEGEN	ss24375871	Sep 20, 2004 (123)
4	ABI	ss42465392	Mar 14, 2006 (126)
5	AFFY	ss65963927	Dec 02, 2006 (127)
6	ILLUMINA	ss66568210	Dec 02, 2006 (127)
7	ILLUMINA	ss67928207	Dec 02, 2006 (127)
8	ILLUMINA	ss68049297	Dec 02, 2006 (127)
9	PERLEGEN	ss68960963	May 18, 2007 (127)
10	ILLUMINA	ss71613961	May 18, 2007 (127)
11	ILLUMINA	ss75592905	Dec 07, 2007 (129)
12	ILLUMINA	ss79299293	Dec 14, 2007 (130)
13	HGSV	ss83551389	Dec 14, 2007 (130)
14	KRIBB_YJKIM	ss83629753	Dec 14, 2007 (130)
15	BCMHGSC_JDW	ss93354721	Mar 24, 2008 (129)
16	ILLUMINA	ss98269746	May 23, 2008 (130)
17	HUMANGENOME_JCVI	ss98792589	Feb 03, 2009 (130)
18	1000GENOMES	ss109667638	Jan 24, 2009 (130)
19	ILLUMINA	ss123009368	Dec 01, 2009 (131)
20	ENSEMBL	ss139645214	Dec 01, 2009 (131)
21	ENSEMBL	ss143658348	Dec 01, 2009 (131)
22	ILLUMINA	ss154499614	Dec 01, 2009 (131)
23	ILLUMINA	ss159673466	Dec 01, 2009 (131)
24	ILLUMINA	ss160996726	Dec 01, 2009 (131)
25	ILLUMINA	ss172477500	Jul 04, 2010 (132)
26	ILLUMINA	ss174862182	Jul 04, 2010 (132)
27	BUSHMAN	ss201279181	Jul 04, 2010 (132)
28	BCM-HGSC-SUB	ss206858643	Jul 04, 2010 (132)
29	1000GENOMES	ss222147839	Jul 14, 2010 (132)
30	1000GENOMES	ss233278845	Jul 14, 2010 (132)
31	1000GENOMES	ss240374238	Jul 15, 2010 (132)
32	PJP	ss293531760	May 09, 2011 (134)
33	ILLUMINA	ss481927576	May 04, 2012 (137)
34	ILLUMINA	ss481960622	May 04, 2012 (137)
35	ILLUMINA	ss482918495	Sep 08, 2015 (146)
36	ILLUMINA	ss485757567	May 04, 2012 (137)
37	ILLUMINA	ss537609004	Sep 08, 2015 (146)
38	SSMP	ss652839305	Apr 25, 2013 (138)
39	ILLUMINA	ss779013232	Sep 08, 2015 (146)
40	ILLUMINA	ss783324584	Sep 08, 2015 (146)
41	ILLUMINA	ss784276418	Sep 08, 2015 (146)
42	ILLUMINA	ss825629811	Apr 01, 2015 (144)
43	ILLUMINA	ss832586223	Sep 08, 2015 (146)
44	ILLUMINA	ss833184189	Jul 13, 2019 (153)
45	ILLUMINA	ss834475718	Sep 08, 2015 (146)
46	EVA-GONL	ss982471190	Aug 21, 2014 (142)
47	JMKIDD_LAB	ss1073298846	Aug 21, 2014 (142)
48	1000GENOMES	ss1318553366	Aug 21, 2014 (142)
49	HAMMER_LAB	ss1397437492	Sep 08, 2015 (146)
50	DDI	ss1430601708	Apr 01, 2015 (144)
51	EVA_GENOME_DK	ss1581486409	Apr 01, 2015 (144)
52	EVA_DECODE	ss1592014993	Apr 01, 2015 (144)
53	EVA_UK10K_ALSPAC	ss1614727892	Apr 01, 2015 (144)
54	EVA_UK10K_TWINSUK	ss1657721925	Apr 01, 2015 (144)
55	EVA_SVP	ss1712826576	Apr 01, 2015 (144)
56	ILLUMINA	ss1752566922	Sep 08, 2015 (146)
57	HAMMER_LAB	ss1804228233	Sep 08, 2015 (146)
58	WEILL_CORNELL_DGM	ss1925725676	Feb 12, 2016 (147)
59	GENOMED	ss1970284426	Jul 19, 2016 (147)
60	JJLAB	ss2023476858	Sep 14, 2016 (149)
61	USC_VALOUEV	ss2151636923	Dec 20, 2016 (150)
62	HUMAN_LONGEVITY	ss2280935916	Dec 20, 2016 (150)
63	ILLUMINA	ss2634384173	Nov 08, 2017 (151)
64	GRF	ss2707218416	Nov 08, 2017 (151)
65	GNOMAD	ss2834616338	Nov 08, 2017 (151)
66	SWEGEN	ss2998339058	Nov 08, 2017 (151)
67	BIOINF_KMB_FNS_UNIBA	ss3025520859	Nov 08, 2017 (151)
68	CSHL	ss3346781640	Nov 08, 2017 (151)
69	ILLUMINA	ss3629417555	Oct 12, 2018 (152)
70	ILLUMINA	ss3632305279	Oct 12, 2018 (152)
71	ILLUMINA	ss3633401878	Oct 12, 2018 (152)
72	ILLUMINA	ss3634123645	Oct 12, 2018 (152)
73	ILLUMINA	ss3635038803	Oct 12, 2018 (152)
74	ILLUMINA	ss3635805087	Oct 12, 2018 (152)
75	ILLUMINA	ss3636752788	Oct 12, 2018 (152)
76	ILLUMINA	ss3637557787	Oct 12, 2018 (152)
77	ILLUMINA	ss3638600363	Oct 12, 2018 (152)
78	ILLUMINA	ss3639302687	Oct 12, 2018 (152)
79	ILLUMINA	ss3639676117	Oct 12, 2018 (152)
80	ILLUMINA	ss3640746097	Oct 12, 2018 (152)
81	ILLUMINA	ss3643542723	Oct 12, 2018 (152)
82	URBANLAB	ss3648241781	Oct 12, 2018 (152)
83	EGCUT_WGS	ss3666265086	Jul 13, 2019 (153)
84	EVA_DECODE	ss3716367227	Jul 13, 2019 (153)
85	ACPOP	ss3733107148	Jul 13, 2019 (153)
86	ILLUMINA	ss3745338942	Jul 13, 2019 (153)
87	EVA	ss3764478119	Jul 13, 2019 (153)
88	ILLUMINA	ss3772832791	Jul 13, 2019 (153)
89	KHV_HUMAN_GENOMES	ss3807640078	Jul 13, 2019 (153)
90	EVA	ss3829673159	Apr 26, 2020 (154)
91	EVA	ss3838310608	Apr 26, 2020 (154)
92	EVA	ss3843752000	Apr 26, 2020 (154)
93	HGDP	ss3847818616	Apr 26, 2020 (154)
94	SGDP_PRJ	ss3863685367	Apr 26, 2020 (154)
95	KRGDB	ss3910409380	Apr 26, 2020 (154)
96	EVA	ss3984559654	Apr 26, 2021 (155)
97	EVA	ss4017249155	Apr 26, 2021 (155)
98	TOPMED	ss4690275908	Apr 26, 2021 (155)
99	TOMMO_GENOMICS	ss5175676021	Apr 26, 2021 (155)
100	1000G_HIGH_COVERAGE	ss5267026023	Oct 13, 2022 (156)
101	GENOGRAPHIC	ss5314511065	Oct 13, 2022 (156)
102	EVA	ss5315112301	Oct 13, 2022 (156)
103	HUGCELL_USP	ss5464861137	Oct 13, 2022 (156)
104	1000G_HIGH_COVERAGE	ss5552277767	Oct 13, 2022 (156)
105	SANFORD_IMAGENETICS	ss5639552827	Oct 13, 2022 (156)
106	TOMMO_GENOMICS	ss5713198523	Oct 13, 2022 (156)
107	EVA	ss5799672367	Oct 13, 2022 (156)
108	YY_MCH	ss5807055548	Oct 13, 2022 (156)
109	EVA	ss5836103520	Oct 13, 2022 (156)
110	EVA	ss5897677634	Oct 13, 2022 (156)
111	EVA	ss5968046308	Oct 13, 2022 (156)
112	1000Genomes	NC_000005.9 - 178329846	Oct 12, 2018 (152)
113	1000Genomes_30x	NC_000005.10 - 178902845	Oct 13, 2022 (156)
114	The Avon Longitudinal Study of Parents and Children	NC_000005.9 - 178329846	Oct 12, 2018 (152)
115	Genome-wide autozygosity in Daghestan	NC_000005.8 - 178262452	Apr 26, 2020 (154)
116	Genetic variation in the Estonian population	NC_000005.9 - 178329846	Oct 12, 2018 (152)
117	Genographic Project	NC_000005.10 - 178902845	Oct 13, 2022 (156)
118	The Danish reference pan genome	NC_000005.9 - 178329846	Apr 26, 2020 (154)
119	gnomAD - Genomes	NC_000005.10 - 178902845	Apr 26, 2021 (155)
120	Genome of the Netherlands Release 5	NC_000005.9 - 178329846	Apr 26, 2020 (154)
121	HGDP-CEPH-db Supplement 1	NC_000005.8 - 178262452	Apr 26, 2020 (154)
122	HapMap	NC_000005.10 - 178902845	Apr 26, 2020 (154)
123	KOREAN population from KRGDB	NC_000005.9 - 178329846	Apr 26, 2020 (154)
124	Northern Sweden	NC_000005.9 - 178329846	Jul 13, 2019 (153)
125	CNV burdens in cranial meningiomas	NC_000005.9 - 178329846	Apr 26, 2021 (155)
126	Qatari	NC_000005.9 - 178329846	Apr 26, 2020 (154)
127	SGDP_PRJ	NC_000005.9 - 178329846	Apr 26, 2020 (154)
128	Siberian	NC_000005.9 - 178329846	Apr 26, 2020 (154)
129	8.3KJPN	NC_000005.9 - 178329846	Apr 26, 2021 (155)
130	14KJPN	NC_000005.10 - 178902845	Oct 13, 2022 (156)
131	TopMed	NC_000005.10 - 178902845	Apr 26, 2021 (155)
132	UK 10K study - Twins	NC_000005.9 - 178329846	Oct 12, 2018 (152)
133	A Vietnamese Genetic Variation Database	NC_000005.9 - 178329846	Jul 13, 2019 (153)
134	ALFA	NC_000005.10 - 178902845	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)
rs17593179	Oct 08, 2004 (123)
rs56768407	May 23, 2008 (130)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
412245, 496508, ss83551389, ss93354721, ss109667638, ss201279181, ss206858643, ss293531760, ss481927576, ss825629811, ss1397437492, ss1592014993, ss1712826576, ss3639302687, ss3639676117, ss3643542723, ss3847818616	NC_000005.8:178262451:T:C	NC_000005.10:178902844:T:C	(self)
30279657, 16856320, 12003334, 7651348, 7480470, 17586774, 6392013, 109028, 7767606, 15702347, 4153277, 33645328, 16856320, 3733223, ss222147839, ss233278845, ss240374238, ss481960622, ss482918495, ss485757567, ss537609004, ss652839305, ss779013232, ss783324584, ss784276418, ss832586223, ss833184189, ss834475718, ss982471190, ss1073298846, ss1318553366, ss1430601708, ss1581486409, ss1614727892, ss1657721925, ss1752566922, ss1804228233, ss1925725676, ss1970284426, ss2023476858, ss2151636923, ss2634384173, ss2707218416, ss2834616338, ss2998339058, ss3346781640, ss3629417555, ss3632305279, ss3633401878, ss3634123645, ss3635038803, ss3635805087, ss3636752788, ss3637557787, ss3638600363, ss3640746097, ss3666265086, ss3733107148, ss3745338942, ss3764478119, ss3772832791, ss3829673159, ss3838310608, ss3863685367, ss3910409380, ss3984559654, ss4017249155, ss5175676021, ss5315112301, ss5639552827, ss5799672367, ss5836103520, ss5968046308	NC_000005.9:178329845:T:C	NC_000005.10:178902844:T:C	(self)
39803702, 24911, 214146979, 3037278, 47035627, 527653465, 665917782, ss2280935916, ss3025520859, ss3648241781, ss3716367227, ss3807640078, ss3843752000, ss4690275908, ss5267026023, ss5314511065, ss5464861137, ss5552277767, ss5713198523, ss5807055548, ss5897677634	NC_000005.10:178902844:T:C	NC_000005.10:178902844:T:C	(self)
ss1398209, ss24375871, ss42465392, ss65963927, ss66568210, ss67928207, ss68049297, ss68960963, ss71613961, ss75592905, ss79299293, ss83629753, ss98269746, ss98792589, ss123009368, ss139645214, ss143658348, ss154499614, ss159673466, ss160996726, ss172477500, ss174862182	NT_023133.13:23141118:T:C	NC_000005.10:178902844:T:C	(self)
ss17051124	NT_077451.3:1425051:T:C	NC_000005.10:178902844:T:C	(self)

Publications tab displays PubMed articles citing the variation as a listing of PMID, Title, Author, Year, Journal, ordered by Year, descending.

2 citations for rs953741

PMID	Title	Author	Year	Journal
25819021	A review of pharmacogenetic studies of substance-related disorders.	Jones JD et al.	2015	Drug and alcohol dependence
29623639	Pharmacogenetics of Opioid Use Disorder Treatment.	Crist RC et al.	2018	CNS drugs

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

rs953741