Name: rs10689115
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.

rs10689115

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr12:75400918-75400930 (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: delAT / dupAT / dupATAT
Variation Type: Indel Insertion and Deletion
Frequency: dupAT=0.3362 (2321/6904, ALFA)
(TA)₆T=0.4685 (2346/5008, 1000G)
(TA)₆T=0.4751 (2081/4380, Estonian) (+ 2 more)
(TA)₆T=0.444 (95/214, Vietnamese)
(TA)₆T=0.47 (19/40, GENOME_DK)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: GLIPR1L2 : 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: 20231103111315

Population	Group	Sample Size	Ref Allele	Alt Allele	Ref HMOZ	Alt HMOZ	HTRZ	HWEP
Total	Global	6904	TATATATATATAT=0.6564	TATATATATAT=0.0000, TATATATATATATAT=0.3362, TATATATATATATATAT=0.0074	0.508674	0.183181	0.308145	32
European	Sub	6018	TATATATATATAT=0.6068	TATATATATAT=0.0000, TATATATATATATAT=0.3847, TATATATATATATATAT=0.0085	0.436444	0.209939	0.353617	32
African	Sub	602	TATATATATATAT=1.000	TATATATATAT=0.000, TATATATATATATAT=0.000, TATATATATATATATAT=0.000	1.0	0.0	0.0	N/A
African Others	Sub	34	TATATATATATAT=1.00	TATATATATAT=0.00, TATATATATATATAT=0.00, TATATATATATATATAT=0.00	1.0	0.0	0.0	N/A
African American	Sub	568	TATATATATATAT=1.000	TATATATATAT=0.000, TATATATATATATAT=0.000, TATATATATATATATAT=0.000	1.0	0.0	0.0	N/A
Asian	Sub	26	TATATATATATAT=1.00	TATATATATAT=0.00, TATATATATATATAT=0.00, TATATATATATATATAT=0.00	1.0	0.0	0.0	N/A
East Asian	Sub	24	TATATATATATAT=1.00	TATATATATAT=0.00, TATATATATATATAT=0.00, TATATATATATATATAT=0.00	1.0	0.0	0.0	N/A
Other Asian	Sub	2	TATATATATATAT=1.0	TATATATATAT=0.0, TATATATATATATAT=0.0, TATATATATATATATAT=0.0	1.0	0.0	0.0	N/A
Latin American 1	Sub	36	TATATATATATAT=1.00	TATATATATAT=0.00, TATATATATATATAT=0.00, TATATATATATATATAT=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	106	TATATATATATAT=1.000	TATATATATAT=0.000, TATATATATATATAT=0.000, TATATATATATATATAT=0.000	1.0	0.0	0.0	N/A
South Asian	Sub	30	TATATATATATAT=1.00	TATATATATAT=0.00, TATATATATATATAT=0.00, TATATATATATATATAT=0.00	1.0	0.0	0.0	N/A
Other	Sub	86	TATATATATATAT=0.93	TATATATATAT=0.00, TATATATATATATAT=0.07, TATATATATATATATAT=0.00	0.906977	0.046512	0.046512	10

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
Allele Frequency Aggregator	Total	Global	6904	(TA)₆T=0.6564	delAT=0.0000, dupAT=0.3362, dupATAT=0.0074
Allele Frequency Aggregator	European	Sub	6018	(TA)₆T=0.6068	delAT=0.0000, dupAT=0.3847, dupATAT=0.0085
Allele Frequency Aggregator	African	Sub	602	(TA)₆T=1.000	delAT=0.000, dupAT=0.000, dupATAT=0.000
Allele Frequency Aggregator	Latin American 2	Sub	106	(TA)₆T=1.000	delAT=0.000, dupAT=0.000, dupATAT=0.000
Allele Frequency Aggregator	Other	Sub	86	(TA)₆T=0.93	delAT=0.00, dupAT=0.07, dupATAT=0.00
Allele Frequency Aggregator	Latin American 1	Sub	36	(TA)₆T=1.00	delAT=0.00, dupAT=0.00, dupATAT=0.00
Allele Frequency Aggregator	South Asian	Sub	30	(TA)₆T=1.00	delAT=0.00, dupAT=0.00, dupATAT=0.00
Allele Frequency Aggregator	Asian	Sub	26	(TA)₆T=1.00	delAT=0.00, dupAT=0.00, dupATAT=0.00
1000Genomes	Global	Study-wide	5008	- No frequency provided	dupAT=0.5315
1000Genomes	African	Sub	1322	- No frequency provided	dupAT=0.5129
1000Genomes	East Asian	Sub	1008	- No frequency provided	dupAT=0.5883
1000Genomes	Europe	Sub	1006	- No frequency provided	dupAT=0.5169
1000Genomes	South Asian	Sub	978	- No frequency provided	dupAT=0.496
1000Genomes	American	Sub	694	- No frequency provided	dupAT=0.556
Genetic variation in the Estonian population	Estonian	Study-wide	4380	- No frequency provided	dupAT=0.5249
A Vietnamese Genetic Variation Database	Global	Study-wide	214	- No frequency provided	dupAT=0.556
The Danish reference pan genome	Danish	Study-wide	40	- No frequency provided	dupAT=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 12	NC_000012.12:g.75400919AT[5]
GRCh38.p14 chr 12	NC_000012.12:g.75400919AT[7]
GRCh38.p14 chr 12	NC_000012.12:g.75400919AT[8]
GRCh37.p13 chr 12	NC_000012.11:g.75794699AT[5]
GRCh37.p13 chr 12	NC_000012.11:g.75794699AT[7]
GRCh37.p13 chr 12	NC_000012.11:g.75794699AT[8]

Gene: GLIPR1L2, GLIPR1 like 2 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
GLIPR1L2 transcript variant 1	NM_001270396.2:c.235-9516… NM_001270396.2:c.235-9516TA[5]	N/A	Intron Variant
GLIPR1L2 transcript variant 2	NM_152436.3:c.235-9516TA[… NM_152436.3:c.235-9516TA[5]	N/A	Intron Variant
GLIPR1L2 transcript variant 3	NR_072995.2:n.	N/A	Intron Variant
GLIPR1L2 transcript variant X6	XM_011537949.2:c.-87-9516… XM_011537949.2:c.-87-9516TA[5]	N/A	Intron Variant
GLIPR1L2 transcript variant X5	XM_024448850.2:c.-179+444… XM_024448850.2:c.-179+444TA[5]	N/A	Intron Variant
GLIPR1L2 transcript variant X1	XM_047428338.1:c.-79-9516… XM_047428338.1:c.-79-9516TA[5]	N/A	Intron Variant
GLIPR1L2 transcript variant X2	XM_047428339.1:c.-209-209… XM_047428339.1:c.-209-2099TA[5]	N/A	Intron Variant
GLIPR1L2 transcript variant X3	XM_047428341.1:c.-210+444… XM_047428341.1:c.-210+444TA[5]	N/A	Intron Variant
GLIPR1L2 transcript variant X4	XM_047428342.1:c.-261+444… XM_047428342.1:c.-261+444TA[5]	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	(TA)₆T=	delAT	dupAT	dupATAT
GRCh38.p14 chr 12	NC_000012.12:g.75400918_75400930=	NC_000012.12:g.75400919AT[5]	NC_000012.12:g.75400919AT[7]	NC_000012.12:g.75400919AT[8]
GRCh37.p13 chr 12	NC_000012.11:g.75794698_75794710=	NC_000012.11:g.75794699AT[5]	NC_000012.11:g.75794699AT[7]	NC_000012.11:g.75794699AT[8]
GLIPR1L2 transcript variant 1	NM_001270396.1:c.235-9516=	NM_001270396.1:c.235-9516TA[5]	NM_001270396.1:c.235-9516TA[7]	NM_001270396.1:c.235-9516TA[8]
GLIPR1L2 transcript variant 1	NM_001270396.2:c.235-9516=	NM_001270396.2:c.235-9516TA[5]	NM_001270396.2:c.235-9516TA[7]	NM_001270396.2:c.235-9516TA[8]
GLIPR1L2 transcript variant 2	NM_152436.2:c.235-9516=	NM_152436.2:c.235-9516TA[5]	NM_152436.2:c.235-9516TA[7]	NM_152436.2:c.235-9516TA[8]
GLIPR1L2 transcript variant 2	NM_152436.3:c.235-9516=	NM_152436.3:c.235-9516TA[5]	NM_152436.3:c.235-9516TA[7]	NM_152436.3:c.235-9516TA[8]
GLIPR1L2 transcript variant X1	XM_005268666.1:c.39+9350=	XM_005268666.1:c.39+9350TA[5]	XM_005268666.1:c.39+9350TA[7]	XM_005268666.1:c.39+9350TA[8]
GLIPR1L2 transcript variant X6	XM_011537949.2:c.-87-9516=	XM_011537949.2:c.-87-9516TA[5]	XM_011537949.2:c.-87-9516TA[7]	XM_011537949.2:c.-87-9516TA[8]
GLIPR1L2 transcript variant X5	XM_024448850.2:c.-179+444=	XM_024448850.2:c.-179+444TA[5]	XM_024448850.2:c.-179+444TA[7]	XM_024448850.2:c.-179+444TA[8]
GLIPR1L2 transcript variant X1	XM_047428338.1:c.-79-9516=	XM_047428338.1:c.-79-9516TA[5]	XM_047428338.1:c.-79-9516TA[7]	XM_047428338.1:c.-79-9516TA[8]
GLIPR1L2 transcript variant X2	XM_047428339.1:c.-209-2099=	XM_047428339.1:c.-209-2099TA[5]	XM_047428339.1:c.-209-2099TA[7]	XM_047428339.1:c.-209-2099TA[8]
GLIPR1L2 transcript variant X3	XM_047428341.1:c.-210+444=	XM_047428341.1:c.-210+444TA[5]	XM_047428341.1:c.-210+444TA[7]	XM_047428341.1:c.-210+444TA[8]
GLIPR1L2 transcript variant X4	XM_047428342.1:c.-261+444=	XM_047428342.1:c.-261+444TA[5]	XM_047428342.1:c.-261+444TA[7]	XM_047428342.1:c.-261+444TA[8]

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#.

58 SubSNP, 21 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	HGSV	ss79923507	Dec 14, 2007 (130)
2	HGSV	ss82377598	Dec 14, 2007 (130)
3	HUMANGENOME_JCVI	ss95601068	Feb 05, 2009 (130)
4	BL	ss256124046	May 09, 2011 (134)
5	GMI	ss289138044	May 04, 2012 (138)
6	1000GENOMES	ss327455518	May 09, 2011 (134)
7	1000GENOMES	ss327551004	May 09, 2011 (134)
8	1000GENOMES	ss328000476	May 09, 2011 (134)
9	LUNTER	ss552230350	Apr 25, 2013 (138)
10	LUNTER	ss552515083	Apr 25, 2013 (138)
11	LUNTER	ss553493038	Apr 25, 2013 (138)
12	SSMP	ss664139828	Apr 01, 2015 (144)
13	1000GENOMES	ss1372325829	Aug 21, 2014 (142)
14	DDI	ss1536733321	Apr 01, 2015 (144)
15	EVA_GENOME_DK	ss1574529335	Apr 01, 2015 (144)
16	EVA_DECODE	ss1641799385	Apr 01, 2015 (144)
17	EVA_DECODE	ss1641799386	Apr 01, 2015 (144)
18	EVA_UK10K_ALSPAC	ss1707529893	Apr 01, 2015 (144)
19	EVA_UK10K_ALSPAC	ss1707529895	Apr 01, 2015 (144)
20	EVA_UK10K_TWINSUK	ss1707529966	Apr 01, 2015 (144)
21	EVA_UK10K_TWINSUK	ss1707529969	Apr 01, 2015 (144)
22	GENOMED	ss1967626561	Jul 19, 2016 (147)
23	SWEGEN	ss3009957988	Nov 08, 2017 (151)
24	SWEGEN	ss3009957989	Nov 08, 2017 (151)
25	MCHAISSO	ss3065484975	Nov 08, 2017 (151)
26	BIOINF_KMB_FNS_UNIBA	ss3645262266	Oct 12, 2018 (152)
27	URBANLAB	ss3649872745	Oct 12, 2018 (152)
28	EGCUT_WGS	ss3677232065	Jul 13, 2019 (153)
29	EVA_DECODE	ss3693989996	Jul 13, 2019 (153)
30	EVA_DECODE	ss3693989997	Jul 13, 2019 (153)
31	EVA_DECODE	ss3693989998	Jul 13, 2019 (153)
32	ACPOP	ss3739164986	Jul 13, 2019 (153)
33	ACPOP	ss3739164987	Jul 13, 2019 (153)
34	PACBIO	ss3787271293	Jul 13, 2019 (153)
35	PACBIO	ss3792365400	Jul 13, 2019 (153)
36	PACBIO	ss3797248278	Jul 13, 2019 (153)
37	KHV_HUMAN_GENOMES	ss3816009430	Jul 13, 2019 (153)
38	EVA	ss3833205648	Apr 27, 2020 (154)
39	KOGIC	ss3972256375	Apr 27, 2020 (154)
40	KOGIC	ss3972256376	Apr 27, 2020 (154)
41	GNOMAD	ss4254700035	Apr 26, 2021 (155)
42	GNOMAD	ss4254700036	Apr 26, 2021 (155)
43	GNOMAD	ss4254700037	Apr 26, 2021 (155)
44	TOMMO_GENOMICS	ss5207068068	Apr 26, 2021 (155)
45	TOMMO_GENOMICS	ss5207068069	Apr 26, 2021 (155)
46	1000G_HIGH_COVERAGE	ss5291385483	Oct 16, 2022 (156)
47	1000G_HIGH_COVERAGE	ss5291385484	Oct 16, 2022 (156)
48	HUGCELL_USP	ss5486070392	Oct 16, 2022 (156)
49	HUGCELL_USP	ss5486070393	Oct 16, 2022 (156)
50	EVA	ss5510760816	Oct 16, 2022 (156)
51	SANFORD_IMAGENETICS	ss5653478514	Oct 16, 2022 (156)
52	TOMMO_GENOMICS	ss5757077006	Oct 16, 2022 (156)
53	TOMMO_GENOMICS	ss5757077007	Oct 16, 2022 (156)
54	TOMMO_GENOMICS	ss5757077008	Oct 16, 2022 (156)
55	YY_MCH	ss5813439634	Oct 16, 2022 (156)
56	EVA	ss5838185111	Oct 16, 2022 (156)
57	EVA	ss5838185112	Oct 16, 2022 (156)
58	EVA	ss5850447175	Oct 16, 2022 (156)
59	1000Genomes	NC_000012.11 - 75794698	Oct 12, 2018 (152)
60	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 32447282 (NC_000012.11:75794697::TA 2147/3854) Row 32447283 (NC_000012.11:75794697::TATA 19/3854)	-	Oct 12, 2018 (152)
61	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 32447282 (NC_000012.11:75794697::TA 2147/3854) Row 32447283 (NC_000012.11:75794697::TATA 19/3854)	-	Oct 12, 2018 (152)
62	Genetic variation in the Estonian population	NC_000012.11 - 75794698	Oct 12, 2018 (152)
63	The Danish reference pan genome	NC_000012.11 - 75794698	Apr 27, 2020 (154)
64	gnomAD - Genomes Submission ignored due to conflicting rows: Row 412171373 (NC_000012.12:75400917::TA 73914/138714) Row 412171374 (NC_000012.12:75400917::TATA 544/138780) Row 412171375 (NC_000012.12:75400917:TA: 1/138808)	-	Apr 26, 2021 (155)
65	gnomAD - Genomes Submission ignored due to conflicting rows: Row 412171373 (NC_000012.12:75400917::TA 73914/138714) Row 412171374 (NC_000012.12:75400917::TATA 544/138780) Row 412171375 (NC_000012.12:75400917:TA: 1/138808)	-	Apr 26, 2021 (155)
66	gnomAD - Genomes Submission ignored due to conflicting rows: Row 412171373 (NC_000012.12:75400917::TA 73914/138714) Row 412171374 (NC_000012.12:75400917::TATA 544/138780) Row 412171375 (NC_000012.12:75400917:TA: 1/138808)	-	Apr 26, 2021 (155)
67	Korean Genome Project Submission ignored due to conflicting rows: Row 28634376 (NC_000012.12:75400917::TA 1032/1832) Row 28634377 (NC_000012.12:75400917::TATA 2/1832)	-	Apr 27, 2020 (154)
68	Korean Genome Project Submission ignored due to conflicting rows: Row 28634376 (NC_000012.12:75400917::TA 1032/1832) Row 28634377 (NC_000012.12:75400917::TATA 2/1832)	-	Apr 27, 2020 (154)
69	Northern Sweden Submission ignored due to conflicting rows: Row 12449851 (NC_000012.11:75794697::TA 292/600) Row 12449852 (NC_000012.11:75794697::TATA 2/600)	-	Jul 13, 2019 (153)
70	Northern Sweden Submission ignored due to conflicting rows: Row 12449851 (NC_000012.11:75794697::TA 292/600) Row 12449852 (NC_000012.11:75794697::TATA 2/600)	-	Jul 13, 2019 (153)
71	8.3KJPN Submission ignored due to conflicting rows: Row 65037375 (NC_000012.11:75794697::TA 10059/16760) Row 65037376 (NC_000012.11:75794697::TATA 4/16760)	-	Apr 26, 2021 (155)
72	8.3KJPN Submission ignored due to conflicting rows: Row 65037375 (NC_000012.11:75794697::TA 10059/16760) Row 65037376 (NC_000012.11:75794697::TATA 4/16760)	-	Apr 26, 2021 (155)
73	14KJPN Submission ignored due to conflicting rows: Row 90914110 (NC_000012.12:75400917::TA 16884/28258) Row 90914111 (NC_000012.12:75400917:TA: 1/28258) Row 90914112 (NC_000012.12:75400917::TATA 10/28258)	-	Oct 16, 2022 (156)
74	14KJPN Submission ignored due to conflicting rows: Row 90914110 (NC_000012.12:75400917::TA 16884/28258) Row 90914111 (NC_000012.12:75400917:TA: 1/28258) Row 90914112 (NC_000012.12:75400917::TATA 10/28258)	-	Oct 16, 2022 (156)
75	14KJPN Submission ignored due to conflicting rows: Row 90914110 (NC_000012.12:75400917::TA 16884/28258) Row 90914111 (NC_000012.12:75400917:TA: 1/28258) Row 90914112 (NC_000012.12:75400917::TATA 10/28258)	-	Oct 16, 2022 (156)
76	UK 10K study - Twins Submission ignored due to conflicting rows: Row 32447282 (NC_000012.11:75794697::TA 2036/3708) Row 32447283 (NC_000012.11:75794697::TATA 12/3708)	-	Oct 12, 2018 (152)
77	UK 10K study - Twins Submission ignored due to conflicting rows: Row 32447282 (NC_000012.11:75794697::TA 2036/3708) Row 32447283 (NC_000012.11:75794697::TATA 12/3708)	-	Oct 12, 2018 (152)
78	A Vietnamese Genetic Variation Database	NC_000012.11 - 75794698	Jul 13, 2019 (153)
79	ALFA	NC_000012.12 - 75400918	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)
rs56967167	May 25, 2008 (130)
rs201299094	Apr 25, 2013 (138)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss5510760816, ss5838185112	NC_000012.11:75794697:TA:	NC_000012.12:75400917:TATATATATATA… NC_000012.12:75400917:TATATATATATAT:TATATATATAT
ss3693989996, ss4254700037, ss5757077007	NC_000012.12:75400917:TA:	NC_000012.12:75400917:TATATATATATA… NC_000012.12:75400917:TATATATATATAT:TATATATATAT	(self)
1083084540	NC_000012.12:75400917:TATATATATATA… NC_000012.12:75400917:TATATATATATAT:TATATATATAT	NC_000012.12:75400917:TATATATATATA… NC_000012.12:75400917:TATATATATATAT:TATATATATAT	(self)
ss256124046, ss327455518, ss327551004, ss328000476, ss552230350, ss552515083, ss553493038, ss1641799385	NC_000012.10:74080964::TA	NC_000012.12:75400917:TATATATATATA… NC_000012.12:75400917:TATATATATATAT:TATATATATATATAT	(self)
ss289138044	NC_000012.10:74080977::AT	NC_000012.12:75400917:TATATATATATA… NC_000012.12:75400917:TATATATATATAT:TATATATATATATAT	(self)
58443194, 22970313, 363990, 7202147, ss664139828, ss1372325829, ss1536733321, ss1574529335, ss1707529893, ss1707529966, ss1967626561, ss3009957988, ss3677232065, ss3739164986, ss3787271293, ss3792365400, ss3797248278, ss3833205648, ss5207068068, ss5653478514, ss5838185111	NC_000012.11:75794697::TA	NC_000012.12:75400917:TATATATATATA… NC_000012.12:75400917:TATATATATATAT:TATATATATATATAT	(self)
ss3065484975, ss3645262266, ss3816009430, ss3972256375, ss4254700035, ss5291385483, ss5486070392, ss5757077006, ss5813439634, ss5850447175	NC_000012.12:75400917::TA	NC_000012.12:75400917:TATATATATATA… NC_000012.12:75400917:TATATATATATAT:TATATATATATATAT	(self)
1083084540	NC_000012.12:75400917:TATATATATATA… NC_000012.12:75400917:TATATATATATAT:TATATATATATATAT	NC_000012.12:75400917:TATATATATATA… NC_000012.12:75400917:TATATATATATAT:TATATATATATATAT	(self)
ss3693989997	NC_000012.12:75400919::TA	NC_000012.12:75400917:TATATATATATA… NC_000012.12:75400917:TATATATATATAT:TATATATATATATAT	(self)
ss79923507, ss82377598	NT_029419.12:37938016::AT	NC_000012.12:75400917:TATATATATATA… NC_000012.12:75400917:TATATATATATAT:TATATATATATATAT	(self)
ss1641799386	NC_000012.10:74080964::TATA	NC_000012.12:75400917:TATATATATATA… NC_000012.12:75400917:TATATATATATAT:TATATATATATATATAT	(self)
ss1707529895, ss1707529969, ss3009957989, ss3739164987, ss5207068069	NC_000012.11:75794697::TATA	NC_000012.12:75400917:TATATATATATA… NC_000012.12:75400917:TATATATATATAT:TATATATATATATATAT	(self)
ss3649872745, ss3972256376, ss4254700036, ss5291385484, ss5486070393, ss5757077008	NC_000012.12:75400917::TATA	NC_000012.12:75400917:TATATATATATA… NC_000012.12:75400917:TATATATATATAT:TATATATATATATATAT	(self)
1083084540	NC_000012.12:75400917:TATATATATATA… NC_000012.12:75400917:TATATATATATAT:TATATATATATATATAT	NC_000012.12:75400917:TATATATATATA… NC_000012.12:75400917:TATATATATATAT:TATATATATATATATAT	(self)
ss3693989998	NC_000012.12:75400919::TATA	NC_000012.12:75400917:TATATATATATA… NC_000012.12:75400917:TATATATATATAT:TATATATATATATATAT	(self)
ss95601068	NT_029419.12:37938016::ATAT	NC_000012.12:75400917:TATATATATATA… NC_000012.12:75400917:TATATATATATAT:TATATATATATATATAT	(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 rs10689115

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

rs10689115