Name: rs11315060
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.

rs11315060

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr15:93953824-93953837 (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: del(A)₅ / delAAA / delAA / delA / …
del(A)₅ / delAAA / delAA / delA / dupA / dupAA / dup(A)₄
Variation Type: Indel Insertion and Deletion
Frequency: delA=0.4726 (2383/5042, ALFA)
(A)₁₄=0.2951 (1478/5008, 1000G)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: LINC01580 : Intron Variant
LINC01581 : 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	5042	AAAAAAAAAAAAAA=0.4958	AAAAAAAAA=0.0000, AAAAAAAAAAAA=0.0002, AAAAAAAAAAAAA=0.4726, AAAAAAAAAAAAAAA=0.0313, AAAAAAAAAAAAAAAA=0.0000	0.309152	0.277098	0.413749	32
European	Sub	4864	AAAAAAAAAAAAAA=0.4784	AAAAAAAAA=0.0000, AAAAAAAAAAAA=0.0002, AAAAAAAAAAAAA=0.4893, AAAAAAAAAAAAAAA=0.0321, AAAAAAAAAAAAAAAA=0.0000	0.283713	0.287653	0.428634	25
African	Sub	20	AAAAAAAAAAAAAA=1.00	AAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
African Others	Sub	0	AAAAAAAAAAAAAA=0	AAAAAAAAA=0, AAAAAAAAAAAA=0, AAAAAAAAAAAAA=0, AAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAA=0	0	0	0	N/A
African American	Sub	20	AAAAAAAAAAAAAA=1.00	AAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
Asian	Sub	12	AAAAAAAAAAAAAA=1.00	AAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
East Asian	Sub	8	AAAAAAAAAAAAAA=1.0	AAAAAAAAA=0.0, AAAAAAAAAAAA=0.0, AAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0	1.0	0.0	0.0	N/A
Other Asian	Sub	4	AAAAAAAAAAAAAA=1.0	AAAAAAAAA=0.0, AAAAAAAAAAAA=0.0, AAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0	1.0	0.0	0.0	N/A
Latin American 1	Sub	4	AAAAAAAAAAAAAA=1.0	AAAAAAAAA=0.0, AAAAAAAAAAAA=0.0, AAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0	1.0	0.0	0.0	N/A
Latin American 2	Sub	78	AAAAAAAAAAAAAA=1.00	AAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
South Asian	Sub	14	AAAAAAAAAAAAAA=1.00	AAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
Other	Sub	50	AAAAAAAAAAAAAA=0.90	AAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.06, AAAAAAAAAAAAAAA=0.04, AAAAAAAAAAAAAAAA=0.00	0.913043	0.0	0.086957	0

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	5042	(A)₁₄=0.4958	del(A)₅=0.0000, delAA=0.0002, delA=0.4726, dupA=0.0313, dupAA=0.0000
Allele Frequency Aggregator	European	Sub	4864	(A)₁₄=0.4784	del(A)₅=0.0000, delAA=0.0002, delA=0.4893, dupA=0.0321, dupAA=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	78	(A)₁₄=1.00	del(A)₅=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00
Allele Frequency Aggregator	Other	Sub	50	(A)₁₄=0.90	del(A)₅=0.00, delAA=0.00, delA=0.06, dupA=0.04, dupAA=0.00
Allele Frequency Aggregator	African	Sub	20	(A)₁₄=1.00	del(A)₅=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00
Allele Frequency Aggregator	South Asian	Sub	14	(A)₁₄=1.00	del(A)₅=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00
Allele Frequency Aggregator	Asian	Sub	12	(A)₁₄=1.00	del(A)₅=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00
Allele Frequency Aggregator	Latin American 1	Sub	4	(A)₁₄=1.0	del(A)₅=0.0, delAA=0.0, delA=0.0, dupA=0.0, dupAA=0.0
1000Genomes	Global	Study-wide	5008	(A)₁₄=0.2951	delA=0.7049
1000Genomes	African	Sub	1322	(A)₁₄=0.0635	delA=0.9365
1000Genomes	East Asian	Sub	1008	(A)₁₄=0.4593	delA=0.5407
1000Genomes	Europe	Sub	1006	(A)₁₄=0.2783	delA=0.7217
1000Genomes	South Asian	Sub	978	(A)₁₄=0.453	delA=0.547
1000Genomes	American	Sub	694	(A)₁₄=0.300	delA=0.700

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.93953833_93953837del
GRCh38.p14 chr 15	NC_000015.10:g.93953835_93953837del
GRCh38.p14 chr 15	NC_000015.10:g.93953836_93953837del
GRCh38.p14 chr 15	NC_000015.10:g.93953837del
GRCh38.p14 chr 15	NC_000015.10:g.93953837dup
GRCh38.p14 chr 15	NC_000015.10:g.93953836_93953837dup
GRCh38.p14 chr 15	NC_000015.10:g.93953834_93953837dup
GRCh37.p13 chr 15	NC_000015.9:g.94497062_94497066del
GRCh37.p13 chr 15	NC_000015.9:g.94497064_94497066del
GRCh37.p13 chr 15	NC_000015.9:g.94497065_94497066del
GRCh37.p13 chr 15	NC_000015.9:g.94497066del
GRCh37.p13 chr 15	NC_000015.9:g.94497066dup
GRCh37.p13 chr 15	NC_000015.9:g.94497065_94497066dup
GRCh37.p13 chr 15	NC_000015.9:g.94497063_94497066dup

Gene: LINC01581, long intergenic non-protein coding RNA 1581 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
LINC01581 transcript	NR_120320.1:n.	N/A	Intron Variant

Gene: LINC01580, long intergenic non-protein coding RNA 1580 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
LINC01580 transcript variant 1	NR_120322.1:n.	N/A	Intron Variant
LINC01580 transcript variant 2	NR_120323.1:n.	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	(A)₁₄=	del(A)₅	delAAA	delAA	delA	dupA	dupAA	dup(A)₄
GRCh38.p14 chr 15	NC_000015.10:g.93953824_93953837=	NC_000015.10:g.93953833_93953837del	NC_000015.10:g.93953835_93953837del	NC_000015.10:g.93953836_93953837del	NC_000015.10:g.93953837del	NC_000015.10:g.93953837dup	NC_000015.10:g.93953836_93953837dup	NC_000015.10:g.93953834_93953837dup
GRCh37.p13 chr 15	NC_000015.9:g.94497053_94497066=	NC_000015.9:g.94497062_94497066del	NC_000015.9:g.94497064_94497066del	NC_000015.9:g.94497065_94497066del	NC_000015.9:g.94497066del	NC_000015.9:g.94497066dup	NC_000015.9:g.94497065_94497066dup	NC_000015.9:g.94497063_94497066dup

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#.

54 SubSNP, 20 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	ABI	ss40603030	Mar 15, 2006 (126)
2	HGSV	ss82475984	Sep 08, 2015 (146)
3	HUMANGENOME_JCVI	ss95667521	Dec 05, 2013 (138)
4	BUSHMAN	ss193398168	Jul 04, 2010 (132)
5	GMI	ss287932555	May 09, 2011 (134)
6	GMI	ss289274532	May 04, 2012 (137)
7	PJP	ss294874219	May 09, 2011 (134)
8	PJP	ss294874220	May 09, 2011 (137)
9	SSMP	ss664296158	Apr 01, 2015 (144)
10	1000GENOMES	ss1375322722	Aug 21, 2014 (142)
11	HAMMER_LAB	ss1808339293	Sep 08, 2015 (146)
12	JJLAB	ss2031283259	Sep 14, 2016 (149)
13	SYSTEMSBIOZJU	ss2628764022	Nov 08, 2017 (151)
14	SWEGEN	ss3013785586	Nov 08, 2017 (151)
15	MCHAISSO	ss3063830655	Nov 08, 2017 (151)
16	MCHAISSO	ss3064669613	Nov 08, 2017 (151)
17	MCHAISSO	ss3065602334	Nov 08, 2017 (151)
18	BIOINF_KMB_FNS_UNIBA	ss3645399708	Oct 12, 2018 (152)
19	URBANLAB	ss3650423604	Oct 12, 2018 (152)
20	EVA_DECODE	ss3698500151	Jul 13, 2019 (153)
21	EVA_DECODE	ss3698500152	Jul 13, 2019 (153)
22	EVA_DECODE	ss3698500153	Jul 13, 2019 (153)
23	ACPOP	ss3741187486	Jul 13, 2019 (153)
24	ACPOP	ss3741187487	Jul 13, 2019 (153)
25	PACBIO	ss3787933253	Jul 13, 2019 (153)
26	PACBIO	ss3792931662	Jul 13, 2019 (153)
27	PACBIO	ss3797816328	Jul 13, 2019 (153)
28	KHV_HUMAN_GENOMES	ss3818772647	Jul 13, 2019 (153)
29	EVA	ss3834387290	Apr 27, 2020 (154)
30	EVA	ss3846286969	Apr 27, 2020 (154)
31	KOGIC	ss3976779933	Apr 27, 2020 (154)
32	KOGIC	ss3976779934	Apr 27, 2020 (154)
33	GNOMAD	ss4294115272	Apr 26, 2021 (155)
34	GNOMAD	ss4294115273	Apr 26, 2021 (155)
35	GNOMAD	ss4294115274	Apr 26, 2021 (155)
36	GNOMAD	ss4294115275	Apr 26, 2021 (155)
37	GNOMAD	ss4294115276	Apr 26, 2021 (155)
38	GNOMAD	ss4294115277	Apr 26, 2021 (155)
39	GNOMAD	ss4294115278	Apr 26, 2021 (155)
40	TOMMO_GENOMICS	ss5217632823	Apr 26, 2021 (155)
41	TOMMO_GENOMICS	ss5217632824	Apr 26, 2021 (155)
42	TOMMO_GENOMICS	ss5217632825	Apr 26, 2021 (155)
43	1000G_HIGH_COVERAGE	ss5299526460	Oct 17, 2022 (156)
44	1000G_HIGH_COVERAGE	ss5299526461	Oct 17, 2022 (156)
45	1000G_HIGH_COVERAGE	ss5299526462	Oct 17, 2022 (156)
46	HUGCELL_USP	ss5493130268	Oct 17, 2022 (156)
47	HUGCELL_USP	ss5493130269	Oct 17, 2022 (156)
48	TOMMO_GENOMICS	ss5771873642	Oct 17, 2022 (156)
49	TOMMO_GENOMICS	ss5771873643	Oct 17, 2022 (156)
50	TOMMO_GENOMICS	ss5771873644	Oct 17, 2022 (156)
51	TOMMO_GENOMICS	ss5771873645	Oct 17, 2022 (156)
52	EVA	ss5828620278	Oct 17, 2022 (156)
53	EVA	ss5851419112	Oct 17, 2022 (156)
54	EVA	ss5877113811	Oct 17, 2022 (156)
55	1000Genomes	NC_000015.9 - 94497053	Oct 12, 2018 (152)
56	gnomAD - Genomes Submission ignored due to conflicting rows: Row 478018455 (NC_000015.10:93953823::A 2376/130148) Row 478018456 (NC_000015.10:93953823::AA 2/130204) Row 478018457 (NC_000015.10:93953823::AAAA 1/130204)...	-	Apr 26, 2021 (155)
57	gnomAD - Genomes Submission ignored due to conflicting rows: Row 478018455 (NC_000015.10:93953823::A 2376/130148) Row 478018456 (NC_000015.10:93953823::AA 2/130204) Row 478018457 (NC_000015.10:93953823::AAAA 1/130204)...	-	Apr 26, 2021 (155)
58	gnomAD - Genomes Submission ignored due to conflicting rows: Row 478018455 (NC_000015.10:93953823::A 2376/130148) Row 478018456 (NC_000015.10:93953823::AA 2/130204) Row 478018457 (NC_000015.10:93953823::AAAA 1/130204)...	-	Apr 26, 2021 (155)
59	gnomAD - Genomes Submission ignored due to conflicting rows: Row 478018455 (NC_000015.10:93953823::A 2376/130148) Row 478018456 (NC_000015.10:93953823::AA 2/130204) Row 478018457 (NC_000015.10:93953823::AAAA 1/130204)...	-	Apr 26, 2021 (155)
60	gnomAD - Genomes Submission ignored due to conflicting rows: Row 478018455 (NC_000015.10:93953823::A 2376/130148) Row 478018456 (NC_000015.10:93953823::AA 2/130204) Row 478018457 (NC_000015.10:93953823::AAAA 1/130204)...	-	Apr 26, 2021 (155)
61	gnomAD - Genomes Submission ignored due to conflicting rows: Row 478018455 (NC_000015.10:93953823::A 2376/130148) Row 478018456 (NC_000015.10:93953823::AA 2/130204) Row 478018457 (NC_000015.10:93953823::AAAA 1/130204)...	-	Apr 26, 2021 (155)
62	gnomAD - Genomes Submission ignored due to conflicting rows: Row 478018455 (NC_000015.10:93953823::A 2376/130148) Row 478018456 (NC_000015.10:93953823::AA 2/130204) Row 478018457 (NC_000015.10:93953823::AAAA 1/130204)...	-	Apr 26, 2021 (155)
63	Korean Genome Project Submission ignored due to conflicting rows: Row 33157934 (NC_000015.10:93953823:A: 986/1832) Row 33157935 (NC_000015.10:93953824::A 27/1832)	-	Apr 27, 2020 (154)
64	Korean Genome Project Submission ignored due to conflicting rows: Row 33157934 (NC_000015.10:93953823:A: 986/1832) Row 33157935 (NC_000015.10:93953824::A 27/1832)	-	Apr 27, 2020 (154)
65	Northern Sweden Submission ignored due to conflicting rows: Row 14472351 (NC_000015.9:94497052:A: 347/566) Row 14472352 (NC_000015.9:94497052::A 12/566)	-	Jul 13, 2019 (153)
66	Northern Sweden Submission ignored due to conflicting rows: Row 14472351 (NC_000015.9:94497052:A: 347/566) Row 14472352 (NC_000015.9:94497052::A 12/566)	-	Jul 13, 2019 (153)
67	8.3KJPN Submission ignored due to conflicting rows: Row 75602130 (NC_000015.9:94497052:A: 9696/16758) Row 75602131 (NC_000015.9:94497052:AA: 5/16758) Row 75602132 (NC_000015.9:94497052::A 2/16758)	-	Apr 26, 2021 (155)
68	8.3KJPN Submission ignored due to conflicting rows: Row 75602130 (NC_000015.9:94497052:A: 9696/16758) Row 75602131 (NC_000015.9:94497052:AA: 5/16758) Row 75602132 (NC_000015.9:94497052::A 2/16758)	-	Apr 26, 2021 (155)
69	8.3KJPN Submission ignored due to conflicting rows: Row 75602130 (NC_000015.9:94497052:A: 9696/16758) Row 75602131 (NC_000015.9:94497052:AA: 5/16758) Row 75602132 (NC_000015.9:94497052::A 2/16758)	-	Apr 26, 2021 (155)
70	14KJPN Submission ignored due to conflicting rows: Row 105710746 (NC_000015.10:93953823:A: 16392/28258) Row 105710747 (NC_000015.10:93953823::A 8/28258) Row 105710748 (NC_000015.10:93953823:AA: 9/28258)...	-	Oct 17, 2022 (156)
71	14KJPN Submission ignored due to conflicting rows: Row 105710746 (NC_000015.10:93953823:A: 16392/28258) Row 105710747 (NC_000015.10:93953823::A 8/28258) Row 105710748 (NC_000015.10:93953823:AA: 9/28258)...	-	Oct 17, 2022 (156)
72	14KJPN Submission ignored due to conflicting rows: Row 105710746 (NC_000015.10:93953823:A: 16392/28258) Row 105710747 (NC_000015.10:93953823::A 8/28258) Row 105710748 (NC_000015.10:93953823:AA: 9/28258)...	-	Oct 17, 2022 (156)
73	14KJPN Submission ignored due to conflicting rows: Row 105710746 (NC_000015.10:93953823:A: 16392/28258) Row 105710747 (NC_000015.10:93953823::A 8/28258) Row 105710748 (NC_000015.10:93953823:AA: 9/28258)...	-	Oct 17, 2022 (156)
74	ALFA	NC_000015.10 - 93953824	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)
rs59051568	May 11, 2012 (137)
rs66646306	May 11, 2012 (137)
rs66646307	Feb 26, 2009 (130)
rs67153371	May 11, 2012 (137)
rs67153372	Feb 26, 2009 (130)
rs67153373	Feb 26, 2009 (130)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4294115278	NC_000015.10:93953823:AAAAA:	NC_000015.10:93953823:AAAAAAAAAAAA… NC_000015.10:93953823:AAAAAAAAAAAAAA:AAAAAAAAA	(self)
9911772979	NC_000015.10:93953823:AAAAAAAAAAAA… NC_000015.10:93953823:AAAAAAAAAAAAAA:AAAAAAAAA	NC_000015.10:93953823:AAAAAAAAAAAA… NC_000015.10:93953823:AAAAAAAAAAAAAA:AAAAAAAAA	(self)
ss4294115277, ss5771873645	NC_000015.10:93953823:AAA:	NC_000015.10:93953823:AAAAAAAAAAAA… NC_000015.10:93953823:AAAAAAAAAAAAAA:AAAAAAAAAAA	(self)
ss5217632824	NC_000015.9:94497052:AA:	NC_000015.10:93953823:AAAAAAAAAAAA… NC_000015.10:93953823:AAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
ss3698500153, ss4294115276, ss5299526462, ss5771873644	NC_000015.10:93953823:AA:	NC_000015.10:93953823:AAAAAAAAAAAA… NC_000015.10:93953823:AAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
9911772979	NC_000015.10:93953823:AAAAAAAAAAAA… NC_000015.10:93953823:AAAAAAAAAAAAAA:AAAAAAAAAAAA	NC_000015.10:93953823:AAAAAAAAAAAA… NC_000015.10:93953823:AAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
ss289274532, ss294874219	NC_000015.8:92298056:A:	NC_000015.10:93953823:AAAAAAAAAAAA… NC_000015.10:93953823:AAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss82475984, ss294874220	NC_000015.8:92298069:A:	NC_000015.10:93953823:AAAAAAAAAAAA… NC_000015.10:93953823:AAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
67808448, ss664296158, ss1375322722, ss1808339293, ss2031283259, ss2628764022, ss3013785586, ss3741187486, ss3787933253, ss3792931662, ss3797816328, ss3834387290, ss5217632823, ss5828620278	NC_000015.9:94497052:A:	NC_000015.10:93953823:AAAAAAAAAAAA… NC_000015.10:93953823:AAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss3063830655, ss3064669613, ss3065602334, ss3645399708, ss3650423604, ss3818772647, ss3846286969, ss3976779933, ss4294115275, ss5299526460, ss5493130268, ss5771873642, ss5851419112, ss5877113811	NC_000015.10:93953823:A:	NC_000015.10:93953823:AAAAAAAAAAAA… NC_000015.10:93953823:AAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
9911772979	NC_000015.10:93953823:AAAAAAAAAAAA… NC_000015.10:93953823:AAAAAAAAAAAAAA:AAAAAAAAAAAAA	NC_000015.10:93953823:AAAAAAAAAAAA… NC_000015.10:93953823:AAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss3698500152	NC_000015.10:93953824:A:	NC_000015.10:93953823:AAAAAAAAAAAA… NC_000015.10:93953823:AAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss193398168	NT_010194.18:70676949:A:	NC_000015.10:93953823:AAAAAAAAAAAA… NC_000015.10:93953823:AAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss40603030, ss287932555	NT_010274.17:9462579:A:	NC_000015.10:93953823:AAAAAAAAAAAA… NC_000015.10:93953823:AAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss95667521	NT_010274.17:9462592:A:	NC_000015.10:93953823:AAAAAAAAAAAA… NC_000015.10:93953823:AAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss3741187487, ss5217632825	NC_000015.9:94497052::A	NC_000015.10:93953823:AAAAAAAAAAAA… NC_000015.10:93953823:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss4294115272, ss5299526461, ss5493130269, ss5771873643	NC_000015.10:93953823::A	NC_000015.10:93953823:AAAAAAAAAAAA… NC_000015.10:93953823:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
9911772979	NC_000015.10:93953823:AAAAAAAAAAAA… NC_000015.10:93953823:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	NC_000015.10:93953823:AAAAAAAAAAAA… NC_000015.10:93953823:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss3976779934	NC_000015.10:93953824::A	NC_000015.10:93953823:AAAAAAAAAAAA… NC_000015.10:93953823:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss3698500151	NC_000015.10:93953825::A	NC_000015.10:93953823:AAAAAAAAAAAA… NC_000015.10:93953823:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss4294115273	NC_000015.10:93953823::AA	NC_000015.10:93953823:AAAAAAAAAAAA… NC_000015.10:93953823:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
9911772979	NC_000015.10:93953823:AAAAAAAAAAAA… NC_000015.10:93953823:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	NC_000015.10:93953823:AAAAAAAAAAAA… NC_000015.10:93953823:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss4294115274	NC_000015.10:93953823::AAAA	NC_000015.10:93953823:AAAAAAAAAAAA… NC_000015.10:93953823:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(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 rs11315060

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

rs11315060