Name: rs2247549
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.

rs2247549

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr10:69786817 (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: A>G
Variation Type: SNV Single Nucleotide Variation
Frequency: A=0.117855 (31195/264690, TOPMED)
A=0.078309 (15325/195700, ALFA)
A=0.113931 (15946/139962, GnomAD) (+ 20 more)
A=0.25692 (7260/28258, 14KJPN)
A=0.25483 (4271/16760, 8.3KJPN)
A=0.1736 (1112/6404, 1000G_30x)
A=0.1697 (850/5008, 1000G)
A=0.0761 (341/4480, Estonian)
A=0.0625 (241/3854, ALSPAC)
A=0.0636 (236/3708, TWINSUK)
A=0.2174 (637/2930, KOREAN)
A=0.1579 (329/2084, HGDP_Stanford)
A=0.1744 (330/1892, HapMap)
A=0.2331 (427/1832, Korea1K)
A=0.064 (64/998, GoNL)
A=0.194 (153/790, PRJEB37584)
A=0.073 (44/600, NorthernSweden)
A=0.112 (60/536, SGDP_PRJ)
A=0.125 (27/216, Qatari)
A=0.234 (50/214, Vietnamese)
A=0.04 (4/90, Ancient Sardinia)
A=0.07 (4/56, Siberian)
A=0.03 (1/40, 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	195700	A=0.078309	G=0.921691
European	Sub	169450	A=0.069177	G=0.930823
African	Sub	7064	A=0.1927	G=0.8073
African Others	Sub	264	A=0.239	G=0.761
African American	Sub	6800	A=0.1909	G=0.8091
Asian	Sub	696	A=0.201	G=0.799
East Asian	Sub	552	A=0.221	G=0.779
Other Asian	Sub	144	A=0.125	G=0.875
Latin American 1	Sub	836	A=0.114	G=0.886
Latin American 2	Sub	6902	A=0.0855	G=0.9145
South Asian	Sub	5040	A=0.1688	G=0.8312
Other	Sub	5712	A=0.0991	G=0.9009

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	A=0.117855	G=0.882145
Allele Frequency Aggregator	Total	Global	195700	A=0.078309	G=0.921691
Allele Frequency Aggregator	European	Sub	169450	A=0.069177	G=0.930823
Allele Frequency Aggregator	African	Sub	7064	A=0.1927	G=0.8073
Allele Frequency Aggregator	Latin American 2	Sub	6902	A=0.0855	G=0.9145
Allele Frequency Aggregator	Other	Sub	5712	A=0.0991	G=0.9009
Allele Frequency Aggregator	South Asian	Sub	5040	A=0.1688	G=0.8312
Allele Frequency Aggregator	Latin American 1	Sub	836	A=0.114	G=0.886
Allele Frequency Aggregator	Asian	Sub	696	A=0.201	G=0.799
gnomAD - Genomes	Global	Study-wide	139962	A=0.113931	G=0.886069
gnomAD - Genomes	European	Sub	75896	A=0.07049	G=0.92951
gnomAD - Genomes	African	Sub	41830	A=0.19653	G=0.80347
gnomAD - Genomes	American	Sub	13630	A=0.08437	G=0.91563
gnomAD - Genomes	Ashkenazi Jewish	Sub	3324	A=0.0909	G=0.9091
gnomAD - Genomes	East Asian	Sub	3134	A=0.2195	G=0.7805
gnomAD - Genomes	Other	Sub	2148	A=0.1094	G=0.8906
14KJPN	JAPANESE	Study-wide	28258	A=0.25692	G=0.74308
8.3KJPN	JAPANESE	Study-wide	16760	A=0.25483	G=0.74517
1000Genomes_30x	Global	Study-wide	6404	A=0.1736	G=0.8264
1000Genomes_30x	African	Sub	1786	A=0.2520	G=0.7480
1000Genomes_30x	Europe	Sub	1266	A=0.0529	G=0.9471
1000Genomes_30x	South Asian	Sub	1202	A=0.1839	G=0.8161
1000Genomes_30x	East Asian	Sub	1170	A=0.2385	G=0.7615
1000Genomes_30x	American	Sub	980	A=0.097	G=0.903
1000Genomes	Global	Study-wide	5008	A=0.1697	G=0.8303
1000Genomes	African	Sub	1322	A=0.2405	G=0.7595
1000Genomes	East Asian	Sub	1008	A=0.2351	G=0.7649
1000Genomes	Europe	Sub	1006	A=0.0527	G=0.9473
1000Genomes	South Asian	Sub	978	A=0.181	G=0.819
1000Genomes	American	Sub	694	A=0.094	G=0.906
Genetic variation in the Estonian population	Estonian	Study-wide	4480	A=0.0761	G=0.9239
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	A=0.0625	G=0.9375
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	A=0.0636	G=0.9364
KOREAN population from KRGDB	KOREAN	Study-wide	2930	A=0.2174	G=0.7826
HGDP-CEPH-db Supplement 1	Global	Study-wide	2084	A=0.1579	G=0.8421
HGDP-CEPH-db Supplement 1	Est_Asia	Sub	470	A=0.206	G=0.794
HGDP-CEPH-db Supplement 1	Central_South_Asia	Sub	414	A=0.208	G=0.792
HGDP-CEPH-db Supplement 1	Middle_Est	Sub	350	A=0.071	G=0.929
HGDP-CEPH-db Supplement 1	Europe	Sub	320	A=0.047	G=0.953
HGDP-CEPH-db Supplement 1	Africa	Sub	242	A=0.227	G=0.773
HGDP-CEPH-db Supplement 1	America	Sub	216	A=0.139	G=0.861
HGDP-CEPH-db Supplement 1	Oceania	Sub	72	A=0.29	G=0.71
HapMap	Global	Study-wide	1892	A=0.1744	G=0.8256
HapMap	American	Sub	770	A=0.140	G=0.860
HapMap	African	Sub	692	A=0.218	G=0.782
HapMap	Asian	Sub	254	A=0.240	G=0.760
HapMap	Europe	Sub	176	A=0.057	G=0.943
Korean Genome Project	KOREAN	Study-wide	1832	A=0.2331	G=0.7669
Genome of the Netherlands Release 5	Genome of the Netherlands	Study-wide	998	A=0.064	G=0.936
CNV burdens in cranial meningiomas	Global	Study-wide	790	A=0.194	G=0.806
CNV burdens in cranial meningiomas	CRM	Sub	790	A=0.194	G=0.806
Northern Sweden	ACPOP	Study-wide	600	A=0.073	G=0.927
SGDP_PRJ	Global	Study-wide	536	A=0.112	G=0.888
Qatari	Global	Study-wide	216	A=0.125	G=0.875
A Vietnamese Genetic Variation Database	Global	Study-wide	214	A=0.234	G=0.766
Ancient Sardinia genome-wide 1240k capture data generation and analysis	Global	Study-wide	90	A=0.04	G=0.96
Siberian	Global	Study-wide	56	A=0.07	G=0.93
The Danish reference pan genome	Danish	Study-wide	40	A=0.03	G=0.97

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 10	NC_000010.11:g.69786817A>G
GRCh37.p13 chr 10	NC_000010.10:g.71546573A>G

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	A=	G
GRCh38.p14 chr 10	NC_000010.11:g.69786817=	NC_000010.11:g.69786817A>G
GRCh37.p13 chr 10	NC_000010.10:g.71546573=	NC_000010.10:g.71546573A>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#.

130 SubSNP, 23 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	TSC-CSHL	ss3357181	Sep 28, 2001 (100)
2	SC_JCM	ss3821937	Sep 28, 2001 (100)
3	WI_SSAHASNP	ss12103936	Jul 11, 2003 (116)
4	SC_SNP	ss15558869	Feb 27, 2004 (120)
5	CSHL-HAPMAP	ss17397876	Feb 27, 2004 (120)
6	CSHL-HAPMAP	ss19175468	Feb 27, 2004 (120)
7	SSAHASNP	ss20655571	Apr 05, 2004 (121)
8	ILLUMINA	ss66644270	Dec 01, 2006 (127)
9	ILLUMINA	ss67237683	Dec 01, 2006 (127)
10	ILLUMINA	ss67634031	Dec 01, 2006 (127)
11	ILLUMINA	ss70716010	May 25, 2008 (130)
12	ILLUMINA	ss71283939	May 18, 2007 (127)
13	ILLUMINA	ss75531626	Dec 07, 2007 (129)
14	ILLUMINA	ss79123266	Dec 15, 2007 (130)
15	HGSV	ss81023574	Dec 15, 2007 (130)
16	KRIBB_YJKIM	ss84008163	Dec 15, 2007 (130)
17	BCMHGSC_JDW	ss88260511	Mar 23, 2008 (129)
18	1000GENOMES	ss109544190	Jan 24, 2009 (130)
19	1000GENOMES	ss113438453	Jan 25, 2009 (130)
20	ILLUMINA-UK	ss119214947	Feb 15, 2009 (130)
21	ILLUMINA	ss121966203	Dec 01, 2009 (131)
22	ENSEMBL	ss131939123	Dec 01, 2009 (131)
23	ENSEMBL	ss137941015	Dec 01, 2009 (131)
24	ILLUMINA	ss153893879	Dec 01, 2009 (131)
25	GMI	ss155201678	Dec 01, 2009 (131)
26	ILLUMINA	ss159372357	Dec 01, 2009 (131)
27	ILLUMINA	ss160521553	Dec 01, 2009 (131)
28	COMPLETE_GENOMICS	ss168534105	Jul 04, 2010 (132)
29	COMPLETE_GENOMICS	ss170360907	Jul 04, 2010 (132)
30	ILLUMINA	ss171122232	Jul 04, 2010 (132)
31	ILLUMINA	ss173213827	Jul 04, 2010 (132)
32	COMPLETE_GENOMICS	ss174612090	Jul 04, 2010 (132)
33	BUSHMAN	ss201675447	Jul 04, 2010 (132)
34	BCM-HGSC-SUB	ss207341372	Jul 04, 2010 (132)
35	1000GENOMES	ss224793389	Jul 14, 2010 (132)
36	1000GENOMES	ss235226305	Jul 15, 2010 (132)
37	1000GENOMES	ss241922167	Jul 15, 2010 (132)
38	BL	ss254408416	May 09, 2011 (134)
39	GMI	ss280667546	May 04, 2012 (137)
40	GMI	ss286214291	Apr 25, 2013 (138)
41	PJP	ss290865164	May 09, 2011 (134)
42	ILLUMINA	ss480484634	May 04, 2012 (137)
43	ILLUMINA	ss480499016	May 04, 2012 (137)
44	ILLUMINA	ss481300510	Sep 08, 2015 (146)
45	ILLUMINA	ss485039832	May 04, 2012 (137)
46	ILLUMINA	ss537061853	Sep 08, 2015 (146)
47	TISHKOFF	ss562033303	Apr 25, 2013 (138)
48	SSMP	ss656927333	Apr 25, 2013 (138)
49	ILLUMINA	ss778487601	Sep 08, 2015 (146)
50	ILLUMINA	ss782966144	Sep 08, 2015 (146)
51	ILLUMINA	ss783927953	Sep 08, 2015 (146)
52	ILLUMINA	ss825453784	Jul 19, 2016 (147)
53	ILLUMINA	ss832222418	Sep 08, 2015 (146)
54	ILLUMINA	ss832884175	Jul 13, 2019 (153)
55	ILLUMINA	ss833943559	Sep 08, 2015 (146)
56	EVA-GONL	ss987619290	Aug 21, 2014 (142)
57	JMKIDD_LAB	ss1077084872	Aug 21, 2014 (142)
58	1000GENOMES	ss1337926033	Aug 21, 2014 (142)
59	DDI	ss1426360118	Apr 01, 2015 (144)
60	EVA_GENOME_DK	ss1575196287	Apr 01, 2015 (144)
61	EVA_DECODE	ss1597290737	Apr 01, 2015 (144)
62	EVA_UK10K_ALSPAC	ss1624824475	Apr 01, 2015 (144)
63	EVA_UK10K_TWINSUK	ss1667818508	Apr 01, 2015 (144)
64	EVA_SVP	ss1713188824	Apr 01, 2015 (144)
65	ILLUMINA	ss1751978174	Sep 08, 2015 (146)
66	HAMMER_LAB	ss1806445764	Sep 08, 2015 (146)
67	WEILL_CORNELL_DGM	ss1930984322	Feb 12, 2016 (147)
68	GENOMED	ss1967159939	Jul 19, 2016 (147)
69	JJLAB	ss2026218736	Sep 14, 2016 (149)
70	USC_VALOUEV	ss2154492642	Dec 20, 2016 (150)
71	HUMAN_LONGEVITY	ss2175749896	Dec 20, 2016 (150)
72	SYSTEMSBIOZJU	ss2627579592	Nov 08, 2017 (151)
73	ILLUMINA	ss2632725847	Nov 08, 2017 (151)
74	GRF	ss2698737457	Nov 08, 2017 (151)
75	GNOMAD	ss2890153253	Nov 08, 2017 (151)
76	SWEGEN	ss3006679643	Nov 08, 2017 (151)
77	BIOINF_KMB_FNS_UNIBA	ss3026900748	Nov 08, 2017 (151)
78	CSHL	ss3349182203	Nov 08, 2017 (151)
79	ILLUMINA	ss3626471350	Oct 12, 2018 (152)
80	ILLUMINA	ss3630750669	Oct 12, 2018 (152)
81	ILLUMINA	ss3632953553	Oct 12, 2018 (152)
82	ILLUMINA	ss3633650870	Oct 12, 2018 (152)
83	ILLUMINA	ss3634408792	Oct 12, 2018 (152)
84	ILLUMINA	ss3635343290	Oct 12, 2018 (152)
85	ILLUMINA	ss3636092458	Oct 12, 2018 (152)
86	ILLUMINA	ss3637093970	Oct 12, 2018 (152)
87	ILLUMINA	ss3637856494	Oct 12, 2018 (152)
88	ILLUMINA	ss3638944388	Oct 12, 2018 (152)
89	ILLUMINA	ss3639471975	Oct 12, 2018 (152)
90	ILLUMINA	ss3640116134	Oct 12, 2018 (152)
91	ILLUMINA	ss3641002517	Oct 12, 2018 (152)
92	ILLUMINA	ss3641296807	Oct 12, 2018 (152)
93	ILLUMINA	ss3642859560	Oct 12, 2018 (152)
94	URBANLAB	ss3649402585	Oct 12, 2018 (152)
95	EGCUT_WGS	ss3674095679	Jul 13, 2019 (153)
96	EVA_DECODE	ss3690122321	Jul 13, 2019 (153)
97	ACPOP	ss3737432739	Jul 13, 2019 (153)
98	ILLUMINA	ss3744709656	Jul 13, 2019 (153)
99	EVA	ss3748250531	Jul 13, 2019 (153)
100	ILLUMINA	ss3772210207	Jul 13, 2019 (153)
101	PACBIO	ss3786708968	Jul 13, 2019 (153)
102	PACBIO	ss3791884658	Jul 13, 2019 (153)
103	PACBIO	ss3796766679	Jul 13, 2019 (153)
104	KHV_HUMAN_GENOMES	ss3813626567	Jul 13, 2019 (153)
105	EVA	ss3832190431	Apr 26, 2020 (154)
106	EVA	ss3839635005	Apr 26, 2020 (154)
107	EVA	ss3845107715	Apr 26, 2020 (154)
108	HGDP	ss3847389996	Apr 26, 2020 (154)
109	SGDP_PRJ	ss3874462258	Apr 26, 2020 (154)
110	KRGDB	ss3922548512	Apr 26, 2020 (154)
111	KOGIC	ss3968115082	Apr 26, 2020 (154)
112	EVA	ss3984636143	Apr 26, 2021 (155)
113	EVA	ss3985482064	Apr 26, 2021 (155)
114	EVA	ss4017491715	Apr 26, 2021 (155)
115	TOPMED	ss4856611979	Apr 26, 2021 (155)
116	TOMMO_GENOMICS	ss5198179032	Apr 26, 2021 (155)
117	1000G_HIGH_COVERAGE	ss5284478175	Oct 16, 2022 (156)
118	EVA	ss5315481258	Oct 16, 2022 (156)
119	EVA	ss5394223567	Oct 16, 2022 (156)
120	HUGCELL_USP	ss5480013066	Oct 16, 2022 (156)
121	1000G_HIGH_COVERAGE	ss5578642203	Oct 16, 2022 (156)
122	SANFORD_IMAGENETICS	ss5649536294	Oct 16, 2022 (156)
123	TOMMO_GENOMICS	ss5744167164	Oct 16, 2022 (156)
124	EVA	ss5799815889	Oct 16, 2022 (156)
125	YY_MCH	ss5811639828	Oct 16, 2022 (156)
126	EVA	ss5824567762	Oct 16, 2022 (156)
127	EVA	ss5849621319	Oct 16, 2022 (156)
128	EVA	ss5879392021	Oct 16, 2022 (156)
129	EVA	ss5940811564	Oct 16, 2022 (156)
130	EVA	ss5979329194	Oct 16, 2022 (156)
131	1000Genomes	NC_000010.10 - 71546573	Oct 12, 2018 (152)
132	1000Genomes_30x	NC_000010.11 - 69786817	Oct 16, 2022 (156)
133	The Avon Longitudinal Study of Parents and Children	NC_000010.10 - 71546573	Oct 12, 2018 (152)
134	Genetic variation in the Estonian population	NC_000010.10 - 71546573	Oct 12, 2018 (152)
135	The Danish reference pan genome	NC_000010.10 - 71546573	Apr 26, 2020 (154)
136	gnomAD - Genomes	NC_000010.11 - 69786817	Apr 26, 2021 (155)
137	Genome of the Netherlands Release 5	NC_000010.10 - 71546573	Apr 26, 2020 (154)
138	HGDP-CEPH-db Supplement 1	NC_000010.9 - 71216579	Apr 26, 2020 (154)
139	HapMap	NC_000010.11 - 69786817	Apr 26, 2020 (154)
140	KOREAN population from KRGDB	NC_000010.10 - 71546573	Apr 26, 2020 (154)
141	Korean Genome Project	NC_000010.11 - 69786817	Apr 26, 2020 (154)
142	Northern Sweden	NC_000010.10 - 71546573	Jul 13, 2019 (153)
143	Ancient Sardinia genome-wide 1240k capture data generation and analysis	NC_000010.10 - 71546573	Apr 26, 2021 (155)
144	CNV burdens in cranial meningiomas	NC_000010.10 - 71546573	Apr 26, 2021 (155)
145	Qatari	NC_000010.10 - 71546573	Apr 26, 2020 (154)
146	SGDP_PRJ	NC_000010.10 - 71546573	Apr 26, 2020 (154)
147	Siberian	NC_000010.10 - 71546573	Apr 26, 2020 (154)
148	8.3KJPN	NC_000010.10 - 71546573	Apr 26, 2021 (155)
149	14KJPN	NC_000010.11 - 69786817	Oct 16, 2022 (156)
150	TopMed	NC_000010.11 - 69786817	Apr 26, 2021 (155)
151	UK 10K study - Twins	NC_000010.10 - 71546573	Oct 12, 2018 (152)
152	A Vietnamese Genetic Variation Database	NC_000010.10 - 71546573	Jul 13, 2019 (153)
153	ALFA	NC_000010.11 - 69786817	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)
rs59857443	May 25, 2008 (130)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss81023574, ss3638944388, ss3639471975	NC_000010.8:71216578:A:G	NC_000010.11:69786816:A:G	(self)
67888, ss88260511, ss109544190, ss113438453, ss119214947, ss168534105, ss170360907, ss174612090, ss201675447, ss207341372, ss254408416, ss280667546, ss286214291, ss290865164, ss480484634, ss825453784, ss1597290737, ss1713188824, ss3642859560, ss3847389996	NC_000010.9:71216578:A:G	NC_000010.11:69786816:A:G	(self)
50332439, 27937785, 19833927, 2211021, 12459585, 29725906, 10717604, 707991, 185605, 13026252, 26479238, 7008996, 56148339, 27937785, 6205940, ss224793389, ss235226305, ss241922167, ss480499016, ss481300510, ss485039832, ss537061853, ss562033303, ss656927333, ss778487601, ss782966144, ss783927953, ss832222418, ss832884175, ss833943559, ss987619290, ss1077084872, ss1337926033, ss1426360118, ss1575196287, ss1624824475, ss1667818508, ss1751978174, ss1806445764, ss1930984322, ss1967159939, ss2026218736, ss2154492642, ss2627579592, ss2632725847, ss2698737457, ss2890153253, ss3006679643, ss3349182203, ss3626471350, ss3630750669, ss3632953553, ss3633650870, ss3634408792, ss3635343290, ss3636092458, ss3637093970, ss3637856494, ss3640116134, ss3641002517, ss3641296807, ss3674095679, ss3737432739, ss3744709656, ss3748250531, ss3772210207, ss3786708968, ss3791884658, ss3796766679, ss3832190431, ss3839635005, ss3874462258, ss3922548512, ss3984636143, ss3985482064, ss4017491715, ss5198179032, ss5315481258, ss5394223567, ss5649536294, ss5799815889, ss5824567762, ss5940811564, ss5979329194	NC_000010.10:71546572:A:G	NC_000010.11:69786816:A:G	(self)
66168138, 355721299, 430578, 24493083, 78004268, 72157634, 12520935400, ss2175749896, ss3026900748, ss3649402585, ss3690122321, ss3813626567, ss3845107715, ss3968115082, ss4856611979, ss5284478175, ss5480013066, ss5578642203, ss5744167164, ss5811639828, ss5849621319, ss5879392021	NC_000010.11:69786816:A:G	NC_000010.11:69786816:A:G	(self)
ss12103936	NT_008583.15:20097720:A:G	NC_000010.11:69786816:A:G	(self)
ss15558869, ss17397876, ss19175468, ss20655571	NT_008583.16:20097727:A:G	NC_000010.11:69786816:A:G	(self)
ss3357181, ss3821937, ss66644270, ss67237683, ss67634031, ss70716010, ss71283939, ss75531626, ss79123266, ss84008163, ss121966203, ss131939123, ss137941015, ss153893879, ss155201678, ss159372357, ss160521553, ss171122232, ss173213827	NT_030059.13:22351036:A:G	NC_000010.11:69786816:A: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 rs2247549

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

rs2247549