Name: rs7186041
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.

rs7186041

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr16:49459592 (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: C>T
Variation Type: SNV Single Nucleotide Variation
Frequency: T=0.326756 (86489/264690, TOPMED)
T=0.305086 (63946/209600, ALFA)
T=0.324293 (45416/140046, GnomAD) (+ 21 more)
T=0.34323 (9699/28258, 14KJPN)
T=0.33938 (5688/16760, 8.3KJPN)
T=0.3448 (2208/6404, 1000G_30x)
T=0.3401 (1703/5008, 1000G)
T=0.2817 (1262/4480, Estonian)
T=0.3142 (1211/3854, ALSPAC)
T=0.3047 (1130/3708, TWINSUK)
T=0.3884 (1138/2930, KOREAN)
T=0.3205 (668/2084, HGDP_Stanford)
T=0.3444 (651/1890, HapMap)
T=0.3941 (722/1832, Korea1K)
T=0.322 (321/998, GoNL)
T=0.492 (308/626, Chileans)
T=0.315 (189/600, NorthernSweden)
C=0.378 (121/320, SGDP_PRJ)
T=0.231 (50/216, Qatari)
T=0.449 (97/216, Vietnamese)
T=0.23 (9/40, GENOME_DK)
C=0.33 (10/30, Siberian)
C=0.50 (14/28, Ancient Sardinia)
T=0.50 (14/28, Ancient Sardinia)

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	209600	C=0.694914	T=0.305086
European	Sub	178650	C=0.701013	T=0.298987
African	Sub	7764	C=0.6325	T=0.3675
African Others	Sub	276	C=0.594	T=0.406
African American	Sub	7488	C=0.6339	T=0.3661
Asian	Sub	748	C=0.574	T=0.426
East Asian	Sub	570	C=0.586	T=0.414
Other Asian	Sub	178	C=0.534	T=0.466
Latin American 1	Sub	986	C=0.708	T=0.292
Latin American 2	Sub	9042	C=0.5979	T=0.4021
South Asian	Sub	5052	C=0.8013	T=0.1987
Other	Sub	7358	C=0.6695	T=0.3305

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	C=0.673244	T=0.326756
Allele Frequency Aggregator	Total	Global	209600	C=0.694914	T=0.305086
Allele Frequency Aggregator	European	Sub	178650	C=0.701013	T=0.298987
Allele Frequency Aggregator	Latin American 2	Sub	9042	C=0.5979	T=0.4021
Allele Frequency Aggregator	African	Sub	7764	C=0.6325	T=0.3675
Allele Frequency Aggregator	Other	Sub	7358	C=0.6695	T=0.3305
Allele Frequency Aggregator	South Asian	Sub	5052	C=0.8013	T=0.1987
Allele Frequency Aggregator	Latin American 1	Sub	986	C=0.708	T=0.292
Allele Frequency Aggregator	Asian	Sub	748	C=0.574	T=0.426
gnomAD - Genomes	Global	Study-wide	140046	C=0.675707	T=0.324293
gnomAD - Genomes	European	Sub	75828	C=0.69147	T=0.30853
gnomAD - Genomes	African	Sub	41962	C=0.64258	T=0.35742
gnomAD - Genomes	American	Sub	13658	C=0.69651	T=0.30349
gnomAD - Genomes	Ashkenazi Jewish	Sub	3320	C=0.7446	T=0.2554
gnomAD - Genomes	East Asian	Sub	3128	C=0.5745	T=0.4255
gnomAD - Genomes	Other	Sub	2150	C=0.6749	T=0.3251
14KJPN	JAPANESE	Study-wide	28258	C=0.65677	T=0.34323
8.3KJPN	JAPANESE	Study-wide	16760	C=0.66062	T=0.33938
1000Genomes_30x	Global	Study-wide	6404	C=0.6552	T=0.3448
1000Genomes_30x	African	Sub	1786	C=0.6433	T=0.3567
1000Genomes_30x	Europe	Sub	1266	C=0.6785	T=0.3215
1000Genomes_30x	South Asian	Sub	1202	C=0.7870	T=0.2130
1000Genomes_30x	East Asian	Sub	1170	C=0.5462	T=0.4538
1000Genomes_30x	American	Sub	980	C=0.615	T=0.385
1000Genomes	Global	Study-wide	5008	C=0.6599	T=0.3401
1000Genomes	African	Sub	1322	C=0.6536	T=0.3464
1000Genomes	East Asian	Sub	1008	C=0.5516	T=0.4484
1000Genomes	Europe	Sub	1006	C=0.6869	T=0.3131
1000Genomes	South Asian	Sub	978	C=0.786	T=0.214
1000Genomes	American	Sub	694	C=0.612	T=0.388
Genetic variation in the Estonian population	Estonian	Study-wide	4480	C=0.7183	T=0.2817
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	C=0.6858	T=0.3142
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	C=0.6953	T=0.3047
KOREAN population from KRGDB	KOREAN	Study-wide	2930	C=0.6116	T=0.3884
HGDP-CEPH-db Supplement 1	Global	Study-wide	2084	C=0.6795	T=0.3205
HGDP-CEPH-db Supplement 1	Est_Asia	Sub	470	C=0.606	T=0.394
HGDP-CEPH-db Supplement 1	Central_South_Asia	Sub	414	C=0.768	T=0.232
HGDP-CEPH-db Supplement 1	Middle_Est	Sub	350	C=0.771	T=0.229
HGDP-CEPH-db Supplement 1	Europe	Sub	320	C=0.734	T=0.266
HGDP-CEPH-db Supplement 1	Africa	Sub	242	C=0.640	T=0.360
HGDP-CEPH-db Supplement 1	America	Sub	216	C=0.380	T=0.620
HGDP-CEPH-db Supplement 1	Oceania	Sub	72	C=0.99	T=0.01
HapMap	Global	Study-wide	1890	C=0.6556	T=0.3444
HapMap	American	Sub	770	C=0.657	T=0.343
HapMap	African	Sub	692	C=0.646	T=0.354
HapMap	Asian	Sub	252	C=0.623	T=0.377
HapMap	Europe	Sub	176	C=0.733	T=0.267
Korean Genome Project	KOREAN	Study-wide	1832	C=0.6059	T=0.3941
Genome of the Netherlands Release 5	Genome of the Netherlands	Study-wide	998	C=0.678	T=0.322
Chileans	Chilean	Study-wide	626	C=0.508	T=0.492
Northern Sweden	ACPOP	Study-wide	600	C=0.685	T=0.315
SGDP_PRJ	Global	Study-wide	320	C=0.378	T=0.622
Qatari	Global	Study-wide	216	C=0.769	T=0.231
A Vietnamese Genetic Variation Database	Global	Study-wide	216	C=0.551	T=0.449
The Danish reference pan genome	Danish	Study-wide	40	C=0.78	T=0.23
Siberian	Global	Study-wide	30	C=0.33	T=0.67
Ancient Sardinia genome-wide 1240k capture data generation and analysis	Global	Study-wide	28	C=0.50	T=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 16	NC_000016.10:g.49459592C>T
GRCh37.p13 chr 16	NC_000016.9:g.49493503C>T

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	C=	T
GRCh38.p14 chr 16	NC_000016.10:g.49459592=	NC_000016.10:g.49459592C>T
GRCh37.p13 chr 16	NC_000016.9:g.49493503=	NC_000016.9:g.49493503C>T

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#.

125 SubSNP, 23 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	BCM_SSAHASNP	ss10807727	Jul 11, 2003 (116)
2	BCM_SSAHASNP	ss14256449	Dec 05, 2003 (119)
3	SSAHASNP	ss21315220	Apr 05, 2004 (123)
4	PERLEGEN	ss24052950	Sep 20, 2004 (123)
5	ABI	ss40720943	Mar 15, 2006 (126)
6	AFFY	ss66084317	Nov 30, 2006 (127)
7	ILLUMINA	ss67552936	Nov 30, 2006 (127)
8	ILLUMINA	ss67928174	Nov 30, 2006 (127)
9	ILLUMINA	ss68272159	Dec 12, 2006 (127)
10	PERLEGEN	ss69343445	May 17, 2007 (127)
11	ILLUMINA	ss70914581	May 26, 2008 (130)
12	ILLUMINA	ss71512989	May 17, 2007 (127)
13	ILLUMINA	ss74952332	Dec 06, 2007 (129)
14	AFFY	ss76029828	Dec 06, 2007 (129)
15	KRIBB_YJKIM	ss84633116	Dec 16, 2007 (130)
16	HGSV	ss85456387	Dec 16, 2007 (130)
17	HUMANGENOME_JCVI	ss96635224	Feb 06, 2009 (130)
18	BGI	ss103292904	Dec 01, 2009 (131)
19	1000GENOMES	ss109309495	Jan 23, 2009 (130)
20	1000GENOMES	ss115059424	Jan 25, 2009 (130)
21	ILLUMINA-UK	ss118245735	Feb 14, 2009 (130)
22	ENSEMBL	ss136742824	Dec 01, 2009 (131)
23	ILLUMINA	ss154410890	Dec 01, 2009 (131)
24	GMI	ss157331931	Dec 01, 2009 (131)
25	ILLUMINA	ss159585991	Dec 01, 2009 (131)
26	ILLUMINA	ss160857509	Dec 01, 2009 (131)
27	COMPLETE_GENOMICS	ss169672149	Jul 04, 2010 (132)
28	AFFY	ss170615156	Jul 04, 2010 (132)
29	COMPLETE_GENOMICS	ss171226189	Jul 04, 2010 (132)
30	ILLUMINA	ss174279957	Jul 04, 2010 (132)
31	BUSHMAN	ss201670227	Jul 04, 2010 (132)
32	1000GENOMES	ss227230744	Jul 14, 2010 (132)
33	1000GENOMES	ss237017504	Jul 15, 2010 (132)
34	1000GENOMES	ss243357954	Jul 15, 2010 (132)
35	BL	ss255688445	May 09, 2011 (134)
36	GMI	ss282525061	May 04, 2012 (137)
37	PJP	ss291839949	May 09, 2011 (134)
38	ILLUMINA	ss481497183	May 04, 2012 (137)
39	ILLUMINA	ss481525779	May 04, 2012 (137)
40	ILLUMINA	ss482502014	Sep 08, 2015 (146)
41	ILLUMINA	ss485543768	May 04, 2012 (137)
42	ILLUMINA	ss537447110	Sep 08, 2015 (146)
43	TISHKOFF	ss564887433	Apr 25, 2013 (138)
44	SSMP	ss660658772	Apr 25, 2013 (138)
45	ILLUMINA	ss778710961	Sep 08, 2015 (146)
46	ILLUMINA	ss783217425	Sep 08, 2015 (146)
47	ILLUMINA	ss784171992	Sep 08, 2015 (146)
48	ILLUMINA	ss832477622	Sep 08, 2015 (146)
49	ILLUMINA	ss833097029	Jul 13, 2019 (153)
50	ILLUMINA	ss834170125	Sep 08, 2015 (146)
51	EVA-GONL	ss992468946	Aug 21, 2014 (142)
52	JMKIDD_LAB	ss1080607480	Aug 21, 2014 (142)
53	1000GENOMES	ss1356166401	Aug 21, 2014 (142)
54	DDI	ss1427841379	Apr 01, 2015 (144)
55	EVA_GENOME_DK	ss1577905801	Apr 01, 2015 (144)
56	EVA_UK10K_ALSPAC	ss1634378130	Apr 01, 2015 (144)
57	EVA_UK10K_TWINSUK	ss1677372163	Apr 01, 2015 (144)
58	EVA_DECODE	ss1696501799	Apr 01, 2015 (144)
59	EVA_SVP	ss1713537470	Apr 01, 2015 (144)
60	ILLUMINA	ss1752192890	Sep 08, 2015 (146)
61	HAMMER_LAB	ss1808505384	Sep 08, 2015 (146)
62	WEILL_CORNELL_DGM	ss1935904502	Feb 12, 2016 (147)
63	GENOMED	ss1968256696	Jul 19, 2016 (147)
64	JJLAB	ss2028733971	Sep 14, 2016 (149)
65	USC_VALOUEV	ss2157169232	Dec 20, 2016 (150)
66	HUMAN_LONGEVITY	ss2211991833	Dec 20, 2016 (150)
67	SYSTEMSBIOZJU	ss2628858751	Nov 08, 2017 (151)
68	ILLUMINA	ss2633314826	Nov 08, 2017 (151)
69	ILLUMINA	ss2635063607	Nov 08, 2017 (151)
70	GRF	ss2701692302	Nov 08, 2017 (151)
71	GNOMAD	ss2942799391	Nov 08, 2017 (151)
72	SWEGEN	ss3014484373	Nov 08, 2017 (151)
73	BIOINF_KMB_FNS_UNIBA	ss3028185764	Nov 08, 2017 (151)
74	CSHL	ss3351443481	Nov 08, 2017 (151)
75	ILLUMINA	ss3627517779	Oct 12, 2018 (152)
76	ILLUMINA	ss3631301385	Oct 12, 2018 (152)
77	ILLUMINA	ss3633119798	Oct 12, 2018 (152)
78	ILLUMINA	ss3633825821	Oct 12, 2018 (152)
79	ILLUMINA	ss3634640959	Oct 12, 2018 (152)
80	ILLUMINA	ss3635514147	Oct 12, 2018 (152)
81	ILLUMINA	ss3636331725	Oct 12, 2018 (152)
82	ILLUMINA	ss3637265575	Oct 12, 2018 (152)
83	ILLUMINA	ss3638123941	Oct 12, 2018 (152)
84	ILLUMINA	ss3639073267	Oct 12, 2018 (152)
85	ILLUMINA	ss3639845525	Oct 12, 2018 (152)
86	ILLUMINA	ss3640348278	Oct 12, 2018 (152)
87	ILLUMINA	ss3641071546	Oct 12, 2018 (152)
88	ILLUMINA	ss3641366990	Oct 12, 2018 (152)
89	ILLUMINA	ss3643105241	Oct 12, 2018 (152)
90	ILLUMINA	ss3643895329	Oct 12, 2018 (152)
91	URBANLAB	ss3650506466	Oct 12, 2018 (152)
92	EGCUT_WGS	ss3681458125	Jul 13, 2019 (153)
93	EVA_DECODE	ss3699224479	Jul 13, 2019 (153)
94	ACPOP	ss3741494389	Jul 13, 2019 (153)
95	ILLUMINA	ss3744941381	Jul 13, 2019 (153)
96	EVA	ss3753912175	Jul 13, 2019 (153)
97	ILLUMINA	ss3772439679	Jul 13, 2019 (153)
98	PACBIO	ss3788034825	Jul 13, 2019 (153)
99	PACBIO	ss3793018414	Jul 13, 2019 (153)
100	PACBIO	ss3797903382	Jul 13, 2019 (153)
101	KHV_HUMAN_GENOMES	ss3819202864	Jul 13, 2019 (153)
102	EVA	ss3834560106	Apr 27, 2020 (154)
103	EVA	ss3840885446	Apr 27, 2020 (154)
104	EVA	ss3846377117	Apr 27, 2020 (154)
105	HGDP	ss3847544302	Apr 27, 2020 (154)
106	SGDP_PRJ	ss3884398911	Apr 27, 2020 (154)
107	KRGDB	ss3933879794	Apr 27, 2020 (154)
108	KOGIC	ss3977551518	Apr 27, 2020 (154)
109	EVA	ss3985755215	Apr 26, 2021 (155)
110	EVA	ss4017734883	Apr 26, 2021 (155)
111	TOPMED	ss5014710418	Apr 26, 2021 (155)
112	TOMMO_GENOMICS	ss5219488722	Apr 26, 2021 (155)
113	1000G_HIGH_COVERAGE	ss5300893166	Oct 17, 2022 (156)
114	EVA	ss5315835923	Oct 17, 2022 (156)
115	EVA	ss5423586660	Oct 17, 2022 (156)
116	HUGCELL_USP	ss5494247975	Oct 17, 2022 (156)
117	1000G_HIGH_COVERAGE	ss5603507248	Oct 17, 2022 (156)
118	SANFORD_IMAGENETICS	ss5658866946	Oct 17, 2022 (156)
119	TOMMO_GENOMICS	ss5774475303	Oct 17, 2022 (156)
120	EVA	ss5799956990	Oct 17, 2022 (156)
121	YY_MCH	ss5815957447	Oct 17, 2022 (156)
122	EVA	ss5846383530	Oct 17, 2022 (156)
123	EVA	ss5851558329	Oct 17, 2022 (156)
124	EVA	ss5899018250	Oct 17, 2022 (156)
125	EVA	ss5950254087	Oct 17, 2022 (156)
126	1000Genomes	NC_000016.9 - 49493503	Oct 12, 2018 (152)
127	1000Genomes_30x	NC_000016.10 - 49459592	Oct 17, 2022 (156)
128	The Avon Longitudinal Study of Parents and Children	NC_000016.9 - 49493503	Oct 12, 2018 (152)
129	Chileans	NC_000016.9 - 49493503	Apr 27, 2020 (154)
130	Genetic variation in the Estonian population	NC_000016.9 - 49493503	Oct 12, 2018 (152)
131	The Danish reference pan genome	NC_000016.9 - 49493503	Apr 27, 2020 (154)
132	gnomAD - Genomes	NC_000016.10 - 49459592	Apr 26, 2021 (155)
133	Genome of the Netherlands Release 5	NC_000016.9 - 49493503	Apr 27, 2020 (154)
134	HGDP-CEPH-db Supplement 1	NC_000016.8 - 48051004	Apr 27, 2020 (154)
135	HapMap	NC_000016.10 - 49459592	Apr 27, 2020 (154)
136	KOREAN population from KRGDB	NC_000016.9 - 49493503	Apr 27, 2020 (154)
137	Korean Genome Project	NC_000016.10 - 49459592	Apr 27, 2020 (154)
138	Northern Sweden	NC_000016.9 - 49493503	Jul 13, 2019 (153)
139	Ancient Sardinia genome-wide 1240k capture data generation and analysis	NC_000016.9 - 49493503	Apr 26, 2021 (155)
140	Qatari	NC_000016.9 - 49493503	Apr 27, 2020 (154)
141	SGDP_PRJ	NC_000016.9 - 49493503	Apr 27, 2020 (154)
142	Siberian	NC_000016.9 - 49493503	Apr 27, 2020 (154)
143	8.3KJPN	NC_000016.9 - 49493503	Apr 26, 2021 (155)
144	14KJPN	NC_000016.10 - 49459592	Oct 17, 2022 (156)
145	TopMed	NC_000016.10 - 49459592	Apr 26, 2021 (155)
146	UK 10K study - Twins	NC_000016.9 - 49493503	Oct 12, 2018 (152)
147	A Vietnamese Genetic Variation Database	NC_000016.9 - 49493503	Jul 13, 2019 (153)
148	ALFA	NC_000016.10 - 49459592	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)
rs12921340	Sep 24, 2004 (123)
rs16947467	Oct 08, 2004 (123)
rs61069936	May 26, 2008 (130)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
222194, ss66084317, ss76029828, ss85456387, ss109309495, ss115059424, ss118245735, ss169672149, ss170615156, ss171226189, ss201670227, ss255688445, ss282525061, ss291839949, ss481497183, ss1696501799, ss1713537470, ss2635063607, ss3639073267, ss3639845525, ss3643105241, ss3643895329, ss3847544302	NC_000016.8:48051003:C:T	NC_000016.10:49459591:C:T	(self)
69326242, 38450534, 167443, 27196373, 4118580, 17149552, 41057188, 14779254, 981142, 17946424, 36415891, 9685586, 77458029, 38450534, 8531702, ss227230744, ss237017504, ss243357954, ss481525779, ss482502014, ss485543768, ss537447110, ss564887433, ss660658772, ss778710961, ss783217425, ss784171992, ss832477622, ss833097029, ss834170125, ss992468946, ss1080607480, ss1356166401, ss1427841379, ss1577905801, ss1634378130, ss1677372163, ss1752192890, ss1808505384, ss1935904502, ss1968256696, ss2028733971, ss2157169232, ss2628858751, ss2633314826, ss2701692302, ss2942799391, ss3014484373, ss3351443481, ss3627517779, ss3631301385, ss3633119798, ss3633825821, ss3634640959, ss3635514147, ss3636331725, ss3637265575, ss3638123941, ss3640348278, ss3641071546, ss3641366990, ss3681458125, ss3741494389, ss3744941381, ss3753912175, ss3772439679, ss3788034825, ss3793018414, ss3797903382, ss3834560106, ss3840885446, ss3884398911, ss3933879794, ss3985755215, ss4017734883, ss5219488722, ss5315835923, ss5423586660, ss5658866946, ss5799956990, ss5846383530, ss5950254087	NC_000016.9:49493502:C:T	NC_000016.10:49459591:C:T	(self)
91033183, 489027822, 1378503, 33929519, 108312407, 230256079, 12295882389, ss2211991833, ss3028185764, ss3650506466, ss3699224479, ss3819202864, ss3846377117, ss3977551518, ss5014710418, ss5300893166, ss5494247975, ss5603507248, ss5774475303, ss5815957447, ss5851558329, ss5899018250	NC_000016.10:49459591:C:T	NC_000016.10:49459591:C:T	(self)
ss24052950, ss40720943, ss67552936, ss67928174, ss68272159, ss69343445, ss70914581, ss71512989, ss74952332, ss84633116, ss96635224, ss103292904, ss136742824, ss154410890, ss157331931, ss159585991, ss160857509, ss174279957	NT_010498.15:3107701:C:T	NC_000016.10:49459591:C:T	(self)
ss10807727	NT_010505.13:1601986:C:T	NC_000016.10:49459591:C:T	(self)
ss14256449, ss21315220	NT_010505.14:1601987:C:T	NC_000016.10:49459591:C:T	(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 rs7186041

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

rs7186041