Name: rs10247566
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.

rs10247566

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr7:129127356 (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>C / A>G / A>T
Variation Type: SNV Single Nucleotide Variation
Frequency: A=0.189459 (50148/264690, TOPMED)
A=0.167367 (27002/161334, GnomAD_exome)
A=0.174604 (24447/140014, GnomAD) (+ 17 more)
A=0.13380 (5295/39574, ALFA)
A=0.14281 (3677/25748, ExAC)
A=0.2356 (1509/6404, 1000G_30x)
A=0.2276 (1140/5008, 1000G)
A=0.1306 (585/4480, Estonian)
A=0.1038 (400/3854, ALSPAC)
A=0.0995 (369/3708, TWINSUK)
A=0.2040 (597/2926, KOREAN)
A=0.1927 (353/1832, Korea1K)
A=0.101 (101/998, GoNL)
A=0.172 (103/600, NorthernSweden)
A=0.464 (248/534, MGP)
A=0.173 (86/498, SGDP_PRJ)
A=0.106 (23/216, Qatari)
A=0.238 (51/214, Vietnamese)
A=0.16 (8/50, Siberian)
A=0.17 (7/40, GENOME_DK)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: LOC407835 : Non Coding Transcript 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	39574	A=0.13380	G=0.86620
European	Sub	30594	A=0.11460	G=0.88540
African	Sub	3732	A=0.2505	G=0.7495
African Others	Sub	132	A=0.288	G=0.712
African American	Sub	3600	A=0.2492	G=0.7508
Asian	Sub	182	A=0.253	G=0.747
East Asian	Sub	124	A=0.250	G=0.750
Other Asian	Sub	58	A=0.26	G=0.74
Latin American 1	Sub	164	A=0.189	G=0.811
Latin American 2	Sub	684	A=0.279	G=0.721
South Asian	Sub	114	A=0.184	G=0.816
Other	Sub	4104	A=0.1377	G=0.8623

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=0.189459	G=0.810541
gnomAD - Exomes	Global	Study-wide	161334	A=0.167367	G=0.832633
gnomAD - Exomes	European	Sub	80022	A=0.10898	G=0.89102
gnomAD - Exomes	Asian	Sub	34692	A=0.18670	G=0.81330
gnomAD - Exomes	American	Sub	24982	A=0.31575	G=0.68425
gnomAD - Exomes	African	Sub	8556	A=0.2779	G=0.7221
gnomAD - Exomes	Ashkenazi Jewish	Sub	8544	A=0.1014	G=0.8986
gnomAD - Exomes	Other	Sub	4538	A=0.1481	G=0.8519
gnomAD - Genomes	Global	Study-wide	140014	A=0.174604	G=0.825396
gnomAD - Genomes	European	Sub	75872	A=0.11129	G=0.88871
gnomAD - Genomes	African	Sub	41920	A=0.26562	G=0.73438
gnomAD - Genomes	American	Sub	13640	A=0.25359	G=0.74641
gnomAD - Genomes	Ashkenazi Jewish	Sub	3322	A=0.1008	G=0.8992
gnomAD - Genomes	East Asian	Sub	3114	A=0.2068	G=0.7932
gnomAD - Genomes	Other	Sub	2146	A=0.2004	G=0.7996
Allele Frequency Aggregator	Total	Global	39574	A=0.13380	G=0.86620
Allele Frequency Aggregator	European	Sub	30594	A=0.11460	G=0.88540
Allele Frequency Aggregator	Other	Sub	4104	A=0.1377	G=0.8623
Allele Frequency Aggregator	African	Sub	3732	A=0.2505	G=0.7495
Allele Frequency Aggregator	Latin American 2	Sub	684	A=0.279	G=0.721
Allele Frequency Aggregator	Asian	Sub	182	A=0.253	G=0.747
Allele Frequency Aggregator	Latin American 1	Sub	164	A=0.189	G=0.811
Allele Frequency Aggregator	South Asian	Sub	114	A=0.184	G=0.816
ExAC	Global	Study-wide	25748	A=0.14281	G=0.85719
ExAC	Europe	Sub	12930	A=0.09196	G=0.90804
ExAC	Asian	Sub	9200	A=0.1754	G=0.8246
ExAC	African	Sub	2678	A=0.2644	G=0.7356
ExAC	American	Sub	680	A=0.196	G=0.804
ExAC	Other	Sub	260	A=0.127	G=0.873
1000Genomes_30x	Global	Study-wide	6404	A=0.2356	G=0.7644
1000Genomes_30x	African	Sub	1786	A=0.3163	G=0.6837
1000Genomes_30x	Europe	Sub	1266	A=0.0987	G=0.9013
1000Genomes_30x	South Asian	Sub	1202	A=0.2213	G=0.7787
1000Genomes_30x	East Asian	Sub	1170	A=0.2316	G=0.7684
1000Genomes_30x	American	Sub	980	A=0.288	G=0.712
1000Genomes	Global	Study-wide	5008	A=0.2276	G=0.7724
1000Genomes	African	Sub	1322	A=0.3026	G=0.6974
1000Genomes	East Asian	Sub	1008	A=0.2262	G=0.7738
1000Genomes	Europe	Sub	1006	A=0.1014	G=0.8986
1000Genomes	South Asian	Sub	978	A=0.220	G=0.780
1000Genomes	American	Sub	694	A=0.281	G=0.719
Genetic variation in the Estonian population	Estonian	Study-wide	4480	A=0.1306	G=0.8694
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	A=0.1038	G=0.8962
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	A=0.0995	G=0.9005
KOREAN population from KRGDB	KOREAN	Study-wide	2926	A=0.2040	C=0.0000, G=0.7960, T=0.0000
Korean Genome Project	KOREAN	Study-wide	1832	A=0.1927	G=0.8073
Genome of the Netherlands Release 5	Genome of the Netherlands	Study-wide	998	A=0.101	G=0.899
Northern Sweden	ACPOP	Study-wide	600	A=0.172	G=0.828
Medical Genome Project healthy controls from Spanish population	Spanish controls	Study-wide	534	A=0.464	G=0.536
SGDP_PRJ	Global	Study-wide	498	A=0.173	G=0.827
Qatari	Global	Study-wide	216	A=0.106	G=0.894
A Vietnamese Genetic Variation Database	Global	Study-wide	214	A=0.238	G=0.762
Siberian	Global	Study-wide	50	A=0.16	G=0.84
The Danish reference pan genome	Danish	Study-wide	40	A=0.17	G=0.82

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 7	NC_000007.14:g.129127356A>C
GRCh38.p14 chr 7	NC_000007.14:g.129127356A>G
GRCh38.p14 chr 7	NC_000007.14:g.129127356A>T
GRCh37.p13 chr 7	NC_000007.13:g.128767410A>C
GRCh37.p13 chr 7	NC_000007.13:g.128767410A>G
GRCh37.p13 chr 7	NC_000007.13:g.128767410A>T

Gene: LOC407835, mitogen-activated protein kinase kinase 2 pseudogene (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
LOC407835 transcript variant 1	NR_002144.1:n.1086A>C	N/A	Non Coding Transcript Variant
LOC407835 transcript variant 1	NR_002144.1:n.1086A>G	N/A	Non Coding Transcript Variant
LOC407835 transcript variant 1	NR_002144.1:n.1086A>T	N/A	Non Coding Transcript Variant
LOC407835 transcript variant 2	NR_172946.1:n.1086A>C	N/A	Non Coding Transcript Variant
LOC407835 transcript variant 2	NR_172946.1:n.1086A>G	N/A	Non Coding Transcript Variant
LOC407835 transcript variant 2	NR_172946.1:n.1086A>T	N/A	Non Coding Transcript 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	A=	C	G	T
GRCh38.p14 chr 7	NC_000007.14:g.129127356=	NC_000007.14:g.129127356A>C	NC_000007.14:g.129127356A>G	NC_000007.14:g.129127356A>T
GRCh37.p13 chr 7	NC_000007.13:g.128767410=	NC_000007.13:g.128767410A>C	NC_000007.13:g.128767410A>G	NC_000007.13:g.128767410A>T
LOC407835 transcript variant 1	NR_002144.1:n.1086=	NR_002144.1:n.1086A>C	NR_002144.1:n.1086A>G	NR_002144.1:n.1086A>T
LOC407835 transcript variant 2	NR_172946.1:n.1086=	NR_172946.1:n.1086A>C	NR_172946.1:n.1086A>G	NR_172946.1:n.1086A>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#.

103 SubSNP, 24 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	WUGSC_SSAHASNP	ss14117358	Dec 05, 2003 (119)
2	SSAHASNP	ss22626174	Apr 05, 2004 (121)
3	ABI	ss42968289	Mar 13, 2006 (126)
4	HGSV	ss84148401	Dec 15, 2007 (130)
5	CORNELL	ss86248641	Mar 23, 2008 (129)
6	BCMHGSC_JDW	ss93765071	Mar 25, 2008 (129)
7	HUMANGENOME_JCVI	ss98185645	Feb 06, 2009 (130)
8	BGI	ss105572578	Feb 06, 2009 (130)
9	ENSEMBL	ss142722138	Dec 01, 2009 (131)
10	ENSEMBL	ss142925467	Dec 01, 2009 (131)
11	GMI	ss155490487	Dec 01, 2009 (131)
12	COMPLETE_GENOMICS	ss162712697	Jul 04, 2010 (132)
13	COMPLETE_GENOMICS	ss167104613	Jul 04, 2010 (132)
14	BUSHMAN	ss198264300	Jul 04, 2010 (132)
15	BCM-HGSC-SUB	ss208463224	Jul 04, 2010 (132)
16	1000GENOMES	ss212113657	Jul 14, 2010 (132)
17	1000GENOMES	ss241079882	Jul 15, 2010 (132)
18	BL	ss254672972	May 09, 2011 (134)
19	GMI	ss279529726	May 04, 2012 (137)
20	GMI	ss285717932	Apr 25, 2013 (138)
21	PJP	ss293965194	May 09, 2011 (134)
22	ILLUMINA	ss484231266	May 04, 2012 (137)
23	ILLUMINA	ss485346286	May 04, 2012 (137)
24	CLINSEQ_SNP	ss491914908	May 04, 2012 (137)
25	ILLUMINA	ss536417521	Sep 08, 2015 (146)
26	TISHKOFF	ss560302202	Apr 25, 2013 (138)
27	SSMP	ss654711831	Apr 25, 2013 (138)
28	ILLUMINA	ss779529173	Sep 08, 2015 (146)
29	ILLUMINA	ss782561615	Sep 08, 2015 (146)
30	ILLUMINA	ss834999718	Sep 08, 2015 (146)
31	EVA-GONL	ss984796726	Aug 21, 2014 (142)
32	JMKIDD_LAB	ss1074980449	Aug 21, 2014 (142)
33	1000GENOMES	ss1327134791	Aug 21, 2014 (142)
34	DDI	ss1431278909	Apr 01, 2015 (144)
35	EVA_GENOME_DK	ss1582400996	Apr 01, 2015 (144)
36	EVA_DECODE	ss1594385365	Apr 01, 2015 (144)
37	EVA_UK10K_ALSPAC	ss1619213268	Apr 01, 2015 (144)
38	EVA_UK10K_TWINSUK	ss1662207301	Apr 01, 2015 (144)
39	EVA_EXAC	ss1688943927	Apr 01, 2015 (144)
40	EVA_MGP	ss1711179634	Apr 01, 2015 (144)
41	HAMMER_LAB	ss1805218322	Sep 08, 2015 (146)
42	WEILL_CORNELL_DGM	ss1928054646	Feb 12, 2016 (147)
43	JJLAB	ss2024715579	Sep 14, 2016 (149)
44	ILLUMINA	ss2094980324	Dec 20, 2016 (150)
45	USC_VALOUEV	ss2152936460	Dec 20, 2016 (150)
46	HUMAN_LONGEVITY	ss2297850270	Dec 20, 2016 (150)
47	SYSTEMSBIOZJU	ss2626845412	Nov 08, 2017 (151)
48	ILLUMINA	ss2634659553	Nov 08, 2017 (151)
49	GRF	ss2708654920	Nov 08, 2017 (151)
50	GNOMAD	ss2736762836	Nov 08, 2017 (151)
51	GNOMAD	ss2747922679	Nov 08, 2017 (151)
52	GNOMAD	ss2859106273	Nov 08, 2017 (151)
53	SWEGEN	ss3002032424	Nov 08, 2017 (151)
54	BIOINF_KMB_FNS_UNIBA	ss3026146720	Nov 08, 2017 (151)
55	CSHL	ss3347842950	Nov 08, 2017 (151)
56	ILLUMINA	ss3629913113	Oct 12, 2018 (152)
57	ILLUMINA	ss3632563834	Oct 12, 2018 (152)
58	OMUKHERJEE_ADBS	ss3646363491	Oct 12, 2018 (152)
59	URBANLAB	ss3648751853	Oct 12, 2018 (152)
60	EGCUT_WGS	ss3669788567	Jul 13, 2019 (153)
61	EVA_DECODE	ss3720689715	Jul 13, 2019 (153)
62	ACPOP	ss3735070607	Jul 13, 2019 (153)
63	EVA	ss3767159512	Jul 13, 2019 (153)
64	PACBIO	ss3785957242	Jul 13, 2019 (153)
65	PACBIO	ss3791236255	Jul 13, 2019 (153)
66	PACBIO	ss3796116406	Jul 13, 2019 (153)
67	KHV_HUMAN_GENOMES	ss3810329506	Jul 13, 2019 (153)
68	EVA	ss3825728646	Apr 26, 2020 (154)
69	EVA	ss3830819327	Apr 26, 2020 (154)
70	EVA	ss3838908683	Apr 26, 2020 (154)
71	EVA	ss3844365110	Apr 26, 2020 (154)
72	SGDP_PRJ	ss3868397106	Apr 26, 2020 (154)
73	KRGDB	ss3915743814	Apr 26, 2020 (154)
74	KOGIC	ss3962578005	Apr 26, 2020 (154)
75	FSA-LAB	ss3984380103	Apr 26, 2021 (155)
76	FSA-LAB	ss3984380104	Apr 26, 2021 (155)
77	EVA	ss3986041370	Apr 26, 2021 (155)
78	EVA	ss3986399140	Apr 26, 2021 (155)
79	TOPMED	ss4763756161	Apr 26, 2021 (155)
80	TOMMO_GENOMICS	ss5185580497	Apr 26, 2021 (155)
81	TOMMO_GENOMICS	ss5185580498	Apr 26, 2021 (155)
82	EVA	ss5237037296	Apr 26, 2021 (155)
83	EVA	ss5237198200	Apr 26, 2021 (155)
84	1000G_HIGH_COVERAGE	ss5274736678	Oct 17, 2022 (156)
85	EVA	ss5315278537	Oct 17, 2022 (156)
86	EVA	ss5376779706	Oct 17, 2022 (156)
87	HUGCELL_USP	ss5471622567	Oct 17, 2022 (156)
88	EVA	ss5509138646	Oct 17, 2022 (156)
89	1000G_HIGH_COVERAGE	ss5563896274	Oct 17, 2022 (156)
90	EVA	ss5624171428	Oct 17, 2022 (156)
91	SANFORD_IMAGENETICS	ss5643987710	Oct 17, 2022 (156)
92	TOMMO_GENOMICS	ss5726571152	Oct 17, 2022 (156)
93	TOMMO_GENOMICS	ss5726571153	Oct 17, 2022 (156)
94	EVA	ss5800142258	Oct 17, 2022 (156)
95	YY_MCH	ss5809092654	Oct 17, 2022 (156)
96	EVA	ss5823525021	Oct 17, 2022 (156)
97	EVA	ss5848692597	Oct 17, 2022 (156)
98	EVA	ss5856096637	Oct 17, 2022 (156)
99	EVA	ss5860882457	Oct 17, 2022 (156)
100	EVA	ss5936536742	Oct 17, 2022 (156)
101	EVA	ss5973185063	Oct 17, 2022 (156)
102	EVA	ss5980461929	Oct 17, 2022 (156)
103	EVA	ss5981245598	Oct 17, 2022 (156)
104	1000Genomes	NC_000007.13 - 128767410	Oct 12, 2018 (152)
105	1000Genomes_30x	NC_000007.14 - 129127356	Oct 17, 2022 (156)
106	The Avon Longitudinal Study of Parents and Children	NC_000007.13 - 128767410	Oct 12, 2018 (152)
107	Genetic variation in the Estonian population	NC_000007.13 - 128767410	Oct 12, 2018 (152)
108	ExAC	NC_000007.13 - 128767410	Oct 12, 2018 (152)
109	The Danish reference pan genome	NC_000007.13 - 128767410	Apr 26, 2020 (154)
110	gnomAD - Genomes	NC_000007.14 - 129127356	Apr 26, 2021 (155)
111	gnomAD - Exomes	NC_000007.13 - 128767410	Jul 13, 2019 (153)
112	Genome of the Netherlands Release 5	NC_000007.13 - 128767410	Apr 26, 2020 (154)
113	KOREAN population from KRGDB	NC_000007.13 - 128767410	Apr 26, 2020 (154)
114	Korean Genome Project	NC_000007.14 - 129127356	Apr 26, 2020 (154)
115	Medical Genome Project healthy controls from Spanish population	NC_000007.13 - 128767410	Apr 26, 2020 (154)
116	Northern Sweden	NC_000007.13 - 128767410	Jul 13, 2019 (153)
117	Qatari	NC_000007.13 - 128767410	Apr 26, 2020 (154)
118	SGDP_PRJ	NC_000007.13 - 128767410	Apr 26, 2020 (154)
119	Siberian	NC_000007.13 - 128767410	Apr 26, 2020 (154)
120	8.3KJPN Submission ignored due to conflicting rows: Row 43549804 (NC_000007.13:128767409:A:G 13136/16756) Row 43549805 (NC_000007.13:128767409:A:T 1/16756)	-	Apr 26, 2021 (155)
121	8.3KJPN Submission ignored due to conflicting rows: Row 43549804 (NC_000007.13:128767409:A:G 13136/16756) Row 43549805 (NC_000007.13:128767409:A:T 1/16756)	-	Apr 26, 2021 (155)
122	14KJPN Submission ignored due to conflicting rows: Row 60408256 (NC_000007.14:129127355:A:G 22091/28256) Row 60408257 (NC_000007.14:129127355:A:T 1/28256)	-	Oct 17, 2022 (156)
123	14KJPN Submission ignored due to conflicting rows: Row 60408256 (NC_000007.14:129127355:A:G 22091/28256) Row 60408257 (NC_000007.14:129127355:A:T 1/28256)	-	Oct 17, 2022 (156)
124	TopMed	NC_000007.14 - 129127356	Apr 26, 2021 (155)
125	UK 10K study - Twins	NC_000007.13 - 128767410	Oct 12, 2018 (152)
126	A Vietnamese Genetic Variation Database	NC_000007.13 - 128767410	Jul 13, 2019 (153)
127	ALFA	NC_000007.14 - 129127356	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)
rs60470367	May 26, 2008 (130)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
22921208, ss2736762836, ss3915743814	NC_000007.13:128767409:A:C	NC_000007.14:129127355:A:C	(self)
ss84148401	NC_000007.11:128361360:A:G	NC_000007.14:129127355:A:G	(self)
ss93765071, ss162712697, ss167104613, ss198264300, ss208463224, ss212113657, ss254672972, ss279529726, ss285717932, ss293965194, ss485346286, ss491914908, ss1594385365, ss2094980324	NC_000007.12:128554645:A:G	NC_000007.14:129127355:A:G	(self)
39178455, 21797589, 15526815, 9025881, 8565934, 5926776, 9727420, 22921208, 295394, 8355472, 10096576, 20414086, 5452814, 21797589, 4856450, ss241079882, ss484231266, ss536417521, ss560302202, ss654711831, ss779529173, ss782561615, ss834999718, ss984796726, ss1074980449, ss1327134791, ss1431278909, ss1582400996, ss1619213268, ss1662207301, ss1688943927, ss1711179634, ss1805218322, ss1928054646, ss2024715579, ss2152936460, ss2626845412, ss2634659553, ss2708654920, ss2736762836, ss2747922679, ss2859106273, ss3002032424, ss3347842950, ss3629913113, ss3632563834, ss3646363491, ss3669788567, ss3735070607, ss3767159512, ss3785957242, ss3791236255, ss3796116406, ss3825728646, ss3830819327, ss3838908683, ss3868397106, ss3915743814, ss3984380103, ss3984380104, ss3986041370, ss3986399140, ss5185580497, ss5315278537, ss5376779706, ss5509138646, ss5624171428, ss5643987710, ss5800142258, ss5823525021, ss5848692597, ss5936536742, ss5973185063, ss5980461929, ss5981245598	NC_000007.13:128767409:A:G	NC_000007.14:129127355:A:G	(self)
51422209, 276644420, 18956006, 601133720, 15618906010, ss2297850270, ss3026146720, ss3648751853, ss3720689715, ss3810329506, ss3844365110, ss3962578005, ss4763756161, ss5237037296, ss5237198200, ss5274736678, ss5471622567, ss5563896274, ss5726571152, ss5809092654, ss5856096637, ss5860882457	NC_000007.14:129127355:A:G	NC_000007.14:129127355:A:G	(self)
ss14117358, ss22626174	NT_007933.13:53943554:A:G	NC_000007.14:129127355:A:G	(self)
ss42968289, ss86248641, ss98185645, ss105572578, ss142722138, ss142925467, ss155490487	NT_007933.15:66800252:A:G	NC_000007.14:129127355:A:G	(self)
22921208, ss3915743814, ss5185580498	NC_000007.13:128767409:A:T	NC_000007.14:129127355:A:T	(self)
ss5726571153	NC_000007.14:129127355:A:T	NC_000007.14:129127355:A:T

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

No publications for rs10247566

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

rs10247566