Name: rs11313287
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.

rs11313287

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr15:84764911-84764919 (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: delTT / delT / dupT / dupTT / dup(…
delTT / delT / dupT / dupTT / dup(T)₆ / dup(T)₉
Variation Type: Indel Insertion and Deletion
Frequency: (T)₉=0.435449 (115259/264690, TOPMED)
(T)₉=0.1430 (716/5008, 1000G)
delT=0.1991 (970/4872, ALFA) (+ 1 more)
delT=0.478 (281/588, NorthernSweden)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: ZNF592 : 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	4872	TTTTTTTTT=0.8009	TTTTTTT=0.0000, TTTTTTTT=0.1991, TTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000	0.690066	0.088259	0.221675	32
European	Sub	4284	TTTTTTTTT=0.7918	TTTTTTT=0.0000, TTTTTTTT=0.2082, TTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000	0.671335	0.087768	0.240896	32
African	Sub	248	TTTTTTTTT=0.774	TTTTTTT=0.000, TTTTTTTT=0.226, TTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000	0.701613	0.153226	0.145161	23
African Others	Sub	10	TTTTTTTTT=0.7	TTTTTTT=0.0, TTTTTTTT=0.3, TTTTTTTTTT=0.0, TTTTTTTTTTTTTTT=0.0	0.4	0.0	0.6	1
African American	Sub	238	TTTTTTTTT=0.777	TTTTTTT=0.000, TTTTTTTT=0.223, TTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000	0.714286	0.159664	0.12605	26
Asian	Sub	6	TTTTTTTTT=0.3	TTTTTTT=0.0, TTTTTTTT=0.7, TTTTTTTTTT=0.0, TTTTTTTTTTTTTTT=0.0	0.333333	0.666667	0.0	2
East Asian	Sub	4	TTTTTTTTT=0.5	TTTTTTT=0.0, TTTTTTTT=0.5, TTTTTTTTTT=0.0, TTTTTTTTTTTTTTT=0.0	0.5	0.5	0.0	1
Other Asian	Sub	2	TTTTTTTTT=0.0	TTTTTTT=0.0, TTTTTTTT=1.0, TTTTTTTTTT=0.0, TTTTTTTTTTTTTTT=0.0	0.0	1.0	0.0	N/A
Latin American 1	Sub	48	TTTTTTTTT=1.00	TTTTTTT=0.00, TTTTTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	148	TTTTTTTTT=1.000	TTTTTTT=0.000, TTTTTTTT=0.000, TTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
South Asian	Sub	26	TTTTTTTTT=0.92	TTTTTTT=0.00, TTTTTTTT=0.08, TTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00	0.923077	0.076923	0.0	8
Other	Sub	112	TTTTTTTTT=0.857	TTTTTTT=0.000, TTTTTTTT=0.143, TTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000	0.803571	0.089286	0.107143	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
TopMed	Global	Study-wide	264690	(T)₉=0.435449	delT=0.564551
1000Genomes	Global	Study-wide	5008	(T)₉=0.1430	delT=0.8570
1000Genomes	African	Sub	1322	(T)₉=0.0340	delT=0.9660
1000Genomes	East Asian	Sub	1008	(T)₉=0.0516	delT=0.9484
1000Genomes	Europe	Sub	1006	(T)₉=0.2177	delT=0.7823
1000Genomes	South Asian	Sub	978	(T)₉=0.223	delT=0.777
1000Genomes	American	Sub	694	(T)₉=0.262	delT=0.738
Allele Frequency Aggregator	Total	Global	4872	(T)₉=0.8009	delTT=0.0000, delT=0.1991, dupT=0.0000, dup(T)₆=0.0000
Allele Frequency Aggregator	European	Sub	4284	(T)₉=0.7918	delTT=0.0000, delT=0.2082, dupT=0.0000, dup(T)₆=0.0000
Allele Frequency Aggregator	African	Sub	248	(T)₉=0.774	delTT=0.000, delT=0.226, dupT=0.000, dup(T)₆=0.000
Allele Frequency Aggregator	Latin American 2	Sub	148	(T)₉=1.000	delTT=0.000, delT=0.000, dupT=0.000, dup(T)₆=0.000
Allele Frequency Aggregator	Other	Sub	112	(T)₉=0.857	delTT=0.000, delT=0.143, dupT=0.000, dup(T)₆=0.000
Allele Frequency Aggregator	Latin American 1	Sub	48	(T)₉=1.00	delTT=0.00, delT=0.00, dupT=0.00, dup(T)₆=0.00
Allele Frequency Aggregator	South Asian	Sub	26	(T)₉=0.92	delTT=0.00, delT=0.08, dupT=0.00, dup(T)₆=0.00
Allele Frequency Aggregator	Asian	Sub	6	(T)₉=0.3	delTT=0.0, delT=0.7, dupT=0.0, dup(T)₆=0.0
Northern Sweden	ACPOP	Study-wide	588	(T)₉=0.522	delT=0.478

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 15	NC_000015.10:g.84764918_84764919del
GRCh38.p14 chr 15	NC_000015.10:g.84764919del
GRCh38.p14 chr 15	NC_000015.10:g.84764919dup
GRCh38.p14 chr 15	NC_000015.10:g.84764918_84764919dup
GRCh38.p14 chr 15	NC_000015.10:g.84764914_84764919dup
GRCh38.p14 chr 15	NC_000015.10:g.84764911_84764919dup
GRCh37.p13 chr 15	NC_000015.9:g.85308149_85308150del
GRCh37.p13 chr 15	NC_000015.9:g.85308150del
GRCh37.p13 chr 15	NC_000015.9:g.85308150dup
GRCh37.p13 chr 15	NC_000015.9:g.85308149_85308150dup
GRCh37.p13 chr 15	NC_000015.9:g.85308145_85308150dup
GRCh37.p13 chr 15	NC_000015.9:g.85308142_85308150dup
ZNF592 RefSeqGene	NG_028094.2:g.21332_21333del
ZNF592 RefSeqGene	NG_028094.2:g.21333del
ZNF592 RefSeqGene	NG_028094.2:g.21333dup
ZNF592 RefSeqGene	NG_028094.2:g.21332_21333dup
ZNF592 RefSeqGene	NG_028094.2:g.21328_21333dup
ZNF592 RefSeqGene	NG_028094.2:g.21325_21333dup

Gene: ZNF592, zinc finger protein 592 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
ZNF592 transcript	NM_014630.3:c.-150+103_-1… NM_014630.3:c.-150+103_-150+104del	N/A	Intron Variant
ZNF592 transcript variant X2	XM_005254996.4:c.-20+103_… XM_005254996.4:c.-20+103_-20+104del	N/A	Intron Variant
ZNF592 transcript variant X1	XM_011522246.3:c.-150+103… XM_011522246.3:c.-150+103_-150+104del	N/A	Intron Variant
ZNF592 transcript variant X3	XM_011522247.3:c.-20+103_… XM_011522247.3:c.-20+103_-20+104del	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)₉=	delTT	delT	dupT	dupTT	dup(T)₆	dup(T)₉
GRCh38.p14 chr 15	NC_000015.10:g.84764911_84764919=	NC_000015.10:g.84764918_84764919del	NC_000015.10:g.84764919del	NC_000015.10:g.84764919dup	NC_000015.10:g.84764918_84764919dup	NC_000015.10:g.84764914_84764919dup	NC_000015.10:g.84764911_84764919dup
GRCh37.p13 chr 15	NC_000015.9:g.85308142_85308150=	NC_000015.9:g.85308149_85308150del	NC_000015.9:g.85308150del	NC_000015.9:g.85308150dup	NC_000015.9:g.85308149_85308150dup	NC_000015.9:g.85308145_85308150dup	NC_000015.9:g.85308142_85308150dup
ZNF592 RefSeqGene	NG_028094.2:g.21325_21333=	NG_028094.2:g.21332_21333del	NG_028094.2:g.21333del	NG_028094.2:g.21333dup	NG_028094.2:g.21332_21333dup	NG_028094.2:g.21328_21333dup	NG_028094.2:g.21325_21333dup
ZNF592 transcript	NM_014630.2:c.-150+96=	NM_014630.2:c.-150+103_-150+104del	NM_014630.2:c.-150+104del	NM_014630.2:c.-150+104dup	NM_014630.2:c.-150+103_-150+104dup	NM_014630.2:c.-150+99_-150+104dup	NM_014630.2:c.-150+96_-150+104dup
ZNF592 transcript	NM_014630.3:c.-150+96=	NM_014630.3:c.-150+103_-150+104del	NM_014630.3:c.-150+104del	NM_014630.3:c.-150+104dup	NM_014630.3:c.-150+103_-150+104dup	NM_014630.3:c.-150+99_-150+104dup	NM_014630.3:c.-150+96_-150+104dup
ZNF592 transcript variant X1	XM_005254996.1:c.-20+96=	XM_005254996.1:c.-20+103_-20+104del	XM_005254996.1:c.-20+104del	XM_005254996.1:c.-20+104dup	XM_005254996.1:c.-20+103_-20+104dup	XM_005254996.1:c.-20+99_-20+104dup	XM_005254996.1:c.-20+96_-20+104dup
ZNF592 transcript variant X2	XM_005254996.4:c.-20+96=	XM_005254996.4:c.-20+103_-20+104del	XM_005254996.4:c.-20+104del	XM_005254996.4:c.-20+104dup	XM_005254996.4:c.-20+103_-20+104dup	XM_005254996.4:c.-20+99_-20+104dup	XM_005254996.4:c.-20+96_-20+104dup
ZNF592 transcript variant X1	XM_011522246.3:c.-150+96=	XM_011522246.3:c.-150+103_-150+104del	XM_011522246.3:c.-150+104del	XM_011522246.3:c.-150+104dup	XM_011522246.3:c.-150+103_-150+104dup	XM_011522246.3:c.-150+99_-150+104dup	XM_011522246.3:c.-150+96_-150+104dup
ZNF592 transcript variant X3	XM_011522247.3:c.-20+96=	XM_011522247.3:c.-20+103_-20+104del	XM_011522247.3:c.-20+104del	XM_011522247.3:c.-20+104dup	XM_011522247.3:c.-20+103_-20+104dup	XM_011522247.3:c.-20+99_-20+104dup	XM_011522247.3:c.-20+96_-20+104dup

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#.

53 SubSNP, 12 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	ABI	ss40543321	Mar 14, 2006 (126)
2	ABI	ss40604763	Dec 03, 2013 (138)
3	HGSV	ss81711529	Sep 08, 2015 (146)
4	HGSV	ss81818029	Sep 08, 2015 (146)
5	HGSV	ss81904667	Sep 08, 2015 (146)
6	HGSV	ss83882626	Sep 08, 2015 (146)
7	HUMANGENOME_JCVI	ss95665561	Feb 13, 2009 (137)
8	BGI	ss104706316	Feb 13, 2009 (137)
9	BGI	ss105477026	Dec 01, 2009 (137)
10	BUSHMAN	ss193394682	Jul 04, 2010 (137)
11	BL	ss256178506	Aug 21, 2014 (142)
12	GMI	ss287931519	May 09, 2011 (137)
13	GMI	ss289270609	May 04, 2012 (137)
14	PJP	ss294870970	May 09, 2011 (137)
15	PJP	ss294870971	May 09, 2011 (134)
16	1000GENOMES	ss327691062	Aug 21, 2014 (142)
17	1000GENOMES	ss328174578	Aug 21, 2014 (142)
18	LUNTER	ss552436852	Apr 25, 2013 (138)
19	LUNTER	ss552765564	Apr 25, 2013 (138)
20	LUNTER	ss553581983	Apr 25, 2013 (138)
21	SSMP	ss664290958	Apr 01, 2015 (144)
22	BILGI_BIOE	ss666656616	Apr 25, 2013 (138)
23	1000GENOMES	ss1375208342	Aug 21, 2014 (142)
24	DDI	ss1536814104	Apr 01, 2015 (144)
25	HAMMER_LAB	ss1808303939	Sep 08, 2015 (146)
26	SYSTEMSBIOZJU	ss2628743339	Nov 08, 2017 (151)
27	MCHAISSO	ss3063827982	Nov 08, 2017 (151)
28	MCHAISSO	ss3064666535	Nov 08, 2017 (151)
29	MCHAISSO	ss3065598966	Nov 08, 2017 (151)
30	BIOINF_KMB_FNS_UNIBA	ss3645395516	Oct 12, 2018 (152)
31	EVA_DECODE	ss3698350574	Jul 13, 2019 (153)
32	EVA_DECODE	ss3698350575	Jul 13, 2019 (153)
33	EVA_DECODE	ss3698350576	Jul 13, 2019 (153)
34	EVA_DECODE	ss3698350577	Jul 13, 2019 (153)
35	EVA_DECODE	ss3698350578	Jul 13, 2019 (153)
36	ACPOP	ss3741122737	Jul 13, 2019 (153)
37	KHV_HUMAN_GENOMES	ss3818677634	Jul 13, 2019 (153)
38	EVA	ss3834348360	Apr 27, 2020 (154)
39	GNOMAD	ss4292877774	Apr 26, 2021 (155)
40	GNOMAD	ss4292877775	Apr 26, 2021 (155)
41	TOPMED	ss4999587939	Apr 26, 2021 (155)
42	TOMMO_GENOMICS	ss5217296008	Apr 26, 2021 (155)
43	TOMMO_GENOMICS	ss5217296009	Apr 26, 2021 (155)
44	TOMMO_GENOMICS	ss5217296010	Apr 26, 2021 (155)
45	1000G_HIGH_COVERAGE	ss5299263358	Oct 16, 2022 (156)
46	HUGCELL_USP	ss5492896856	Oct 16, 2022 (156)
47	HUGCELL_USP	ss5492896858	Oct 16, 2022 (156)
48	TOMMO_GENOMICS	ss5771436649	Oct 16, 2022 (156)
49	TOMMO_GENOMICS	ss5771436651	Oct 16, 2022 (156)
50	TOMMO_GENOMICS	ss5771436652	Oct 16, 2022 (156)
51	EVA	ss5828518051	Oct 16, 2022 (156)
52	EVA	ss5828518052	Oct 16, 2022 (156)
53	EVA	ss5876812044	Oct 16, 2022 (156)
54	1000Genomes	NC_000015.9 - 85308142	Oct 12, 2018 (152)
55	gnomAD - Genomes Submission ignored due to conflicting rows: Row 475917354 (NC_000015.10:84764910::T 69/134330) Row 475917356 (NC_000015.10:84764910:T: 77201/134254)	-	Apr 26, 2021 (155)
56	gnomAD - Genomes Submission ignored due to conflicting rows: Row 475917354 (NC_000015.10:84764910::T 69/134330) Row 475917356 (NC_000015.10:84764910:T: 77201/134254)	-	Apr 26, 2021 (155)
57	Northern Sweden	NC_000015.9 - 85308142	Jul 13, 2019 (153)
58	8.3KJPN Submission ignored due to conflicting rows: Row 75265315 (NC_000015.9:85308141:T: 14048/16760) Row 75265316 (NC_000015.9:85308141::T 10/16760) Row 75265317 (NC_000015.9:85308141:TT: 1/16760)	-	Apr 26, 2021 (155)
59	8.3KJPN Submission ignored due to conflicting rows: Row 75265315 (NC_000015.9:85308141:T: 14048/16760) Row 75265316 (NC_000015.9:85308141::T 10/16760) Row 75265317 (NC_000015.9:85308141:TT: 1/16760)	-	Apr 26, 2021 (155)
60	8.3KJPN Submission ignored due to conflicting rows: Row 75265315 (NC_000015.9:85308141:T: 14048/16760) Row 75265316 (NC_000015.9:85308141::T 10/16760) Row 75265317 (NC_000015.9:85308141:TT: 1/16760)	-	Apr 26, 2021 (155)
61	14KJPN Submission ignored due to conflicting rows: Row 105273753 (NC_000015.10:84764910:T: 23698/28258) Row 105273755 (NC_000015.10:84764910::T 16/28258) Row 105273756 (NC_000015.10:84764910:TT: 1/28258)	-	Oct 16, 2022 (156)
62	14KJPN Submission ignored due to conflicting rows: Row 105273753 (NC_000015.10:84764910:T: 23698/28258) Row 105273755 (NC_000015.10:84764910::T 16/28258) Row 105273756 (NC_000015.10:84764910:TT: 1/28258)	-	Oct 16, 2022 (156)
63	14KJPN Submission ignored due to conflicting rows: Row 105273753 (NC_000015.10:84764910:T: 23698/28258) Row 105273755 (NC_000015.10:84764910::T 16/28258) Row 105273756 (NC_000015.10:84764910:TT: 1/28258)	-	Oct 16, 2022 (156)
64	TopMed	NC_000015.10 - 84764911	Apr 26, 2021 (155)
65	ALFA	NC_000015.10 - 84764911	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)
rs60130894	May 25, 2008 (130)
rs67335078	May 11, 2012 (137)
rs67335079	Feb 27, 2009 (130)
rs72522606	May 11, 2012 (137)
rs373206063	May 13, 2013 (138)
rs71135306	May 11, 2012 (137)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss5217296010	NC_000015.9:85308141:TT:	NC_000015.10:84764910:TTTTTTTTT:TT… NC_000015.10:84764910:TTTTTTTTT:TTTTTTT	(self)
ss5771436652	NC_000015.10:84764910:TT:	NC_000015.10:84764910:TTTTTTTTT:TT… NC_000015.10:84764910:TTTTTTTTT:TTTTTTT	(self)
13462996588	NC_000015.10:84764910:TTTTTTTTT:TT… NC_000015.10:84764910:TTTTTTTTT:TTTTTTT	NC_000015.10:84764910:TTTTTTTTT:TT… NC_000015.10:84764910:TTTTTTTTT:TTTTTTT	(self)
ss256178506, ss289270609, ss294870970, ss327691062, ss328174578, ss552436852, ss552765564, ss553581983	NC_000015.8:83109145:T:	NC_000015.10:84764910:TTTTTTTTT:TT… NC_000015.10:84764910:TTTTTTTTT:TTTTTTTT	(self)
ss81711529, ss81818029, ss81904667, ss83882626, ss294870971	NC_000015.8:83109153:T:	NC_000015.10:84764910:TTTTTTTTT:TT… NC_000015.10:84764910:TTTTTTTTT:TTTTTTTT	(self)
67497138, 14407602, ss664290958, ss666656616, ss1375208342, ss1536814104, ss1808303939, ss2628743339, ss3741122737, ss3834348360, ss5217296008, ss5828518051	NC_000015.9:85308141:T:	NC_000015.10:84764910:TTTTTTTTT:TT… NC_000015.10:84764910:TTTTTTTTT:TTTTTTTT	(self)
215133599, ss3063827982, ss3064666535, ss3065598966, ss3645395516, ss3698350574, ss3818677634, ss4292877775, ss4999587939, ss5299263358, ss5492896856, ss5771436649	NC_000015.10:84764910:T:	NC_000015.10:84764910:TTTTTTTTT:TT… NC_000015.10:84764910:TTTTTTTTT:TTTTTTTT	(self)
13462996588	NC_000015.10:84764910:TTTTTTTTT:TT… NC_000015.10:84764910:TTTTTTTTT:TTTTTTTT	NC_000015.10:84764910:TTTTTTTTT:TT… NC_000015.10:84764910:TTTTTTTTT:TTTTTTTT	(self)
ss193394682	NT_010194.18:61488036:T:	NC_000015.10:84764910:TTTTTTTTT:TT… NC_000015.10:84764910:TTTTTTTTT:TTTTTTTT	(self)
ss287931519	NT_010274.17:273668:T:	NC_000015.10:84764910:TTTTTTTTT:TT… NC_000015.10:84764910:TTTTTTTTT:TTTTTTTT	(self)
ss104706316, ss105477026	NT_010274.17:273675:T:	NC_000015.10:84764910:TTTTTTTTT:TT… NC_000015.10:84764910:TTTTTTTTT:TTTTTTTT	(self)
ss40604763	NT_010274.17:273676:T:	NC_000015.10:84764910:TTTTTTTTT:TT… NC_000015.10:84764910:TTTTTTTTT:TTTTTTTT	(self)
ss5217296009, ss5828518052	NC_000015.9:85308141::T	NC_000015.10:84764910:TTTTTTTTT:TT… NC_000015.10:84764910:TTTTTTTTT:TTTTTTTTTT	(self)
ss4292877774, ss5492896858, ss5771436651, ss5876812044	NC_000015.10:84764910::T	NC_000015.10:84764910:TTTTTTTTT:TT… NC_000015.10:84764910:TTTTTTTTT:TTTTTTTTTT	(self)
13462996588	NC_000015.10:84764910:TTTTTTTTT:TT… NC_000015.10:84764910:TTTTTTTTT:TTTTTTTTTT	NC_000015.10:84764910:TTTTTTTTT:TT… NC_000015.10:84764910:TTTTTTTTT:TTTTTTTTTT	(self)
ss3698350575	NC_000015.10:84764911::T	NC_000015.10:84764910:TTTTTTTTT:TT… NC_000015.10:84764910:TTTTTTTTT:TTTTTTTTTT	(self)
ss40543321	NT_010274.17:273676::T	NC_000015.10:84764910:TTTTTTTTT:TT… NC_000015.10:84764910:TTTTTTTTT:TTTTTTTTTT	(self)
ss95665561	NT_010274.17:273677::T	NC_000015.10:84764910:TTTTTTTTT:TT… NC_000015.10:84764910:TTTTTTTTT:TTTTTTTTTT	(self)
ss3698350576	NC_000015.10:84764911::TT	NC_000015.10:84764910:TTTTTTTTT:TT… NC_000015.10:84764910:TTTTTTTTT:TTTTTTTTTTT	(self)
13462996588	NC_000015.10:84764910:TTTTTTTTT:TT… NC_000015.10:84764910:TTTTTTTTT:TTTTTTTTTTTTTTT	NC_000015.10:84764910:TTTTTTTTT:TT… NC_000015.10:84764910:TTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss3698350577	NC_000015.10:84764911::TTTTTT	NC_000015.10:84764910:TTTTTTTTT:TT… NC_000015.10:84764910:TTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss3698350578	NC_000015.10:84764911::TTTTTTTTT	NC_000015.10:84764910:TTTTTTTTT:TT… NC_000015.10:84764910:TTTTTTTTT:TTTTTTTTTTTTTTTTTT	(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 rs11313287

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

rs11313287