Name: rs11320787
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.

rs11320787

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr11:126226951-126226965 (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: delAAA / delAA / delA / dupA / dup…
delAAA / delAA / delA / dupA / dupAA
Variation Type: Indel Insertion and Deletion
Frequency: (A)₁₅=0.3005 (1505/5008, 1000G)
delAAA=0.000 (0/810, ALFA)
delAA=0.000 (0/810, ALFA) (+ 3 more)
delA=0.000 (0/810, ALFA)
dupA=0.000 (0/810, ALFA)
dupAA=0.000 (0/810, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: FAM118B : 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	HWEP
Total	Global	810	AAAAAAAAAAAAAAA=1.000	AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000	1.0	N/A
European	Sub	636	AAAAAAAAAAAAAAA=1.000	AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000	1.0	N/A
African	Sub	92	AAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00	1.0	N/A
African Others	Sub	2	AAAAAAAAAAAAAAA=1.0	AAAAAAAAAAAA=0.0, AAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAA=0.0	1.0	N/A
African American	Sub	90	AAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Asian	Sub	6	AAAAAAAAAAAAAAA=1.0	AAAAAAAAAAAA=0.0, AAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAA=0.0	1.0	N/A
East Asian	Sub	2	AAAAAAAAAAAAAAA=1.0	AAAAAAAAAAAA=0.0, AAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAA=0.0	1.0	N/A
Other Asian	Sub	4	AAAAAAAAAAAAAAA=1.0	AAAAAAAAAAAA=0.0, AAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAA=0.0	1.0	N/A
Latin American 1	Sub	4	AAAAAAAAAAAAAAA=1.0	AAAAAAAAAAAA=0.0, AAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAA=0.0	1.0	N/A
Latin American 2	Sub	38	AAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00	1.0	N/A
South Asian	Sub	2	AAAAAAAAAAAAAAA=1.0	AAAAAAAAAAAA=0.0, AAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAA=0.0	1.0	N/A
Other	Sub	32	AAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00	1.0	N/A

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
1000Genomes	Global	Study-wide	5008	(A)₁₅=0.3005	delA=0.6995
1000Genomes	African	Sub	1322	(A)₁₅=0.2648	delA=0.7352
1000Genomes	East Asian	Sub	1008	(A)₁₅=0.2659	delA=0.7341
1000Genomes	Europe	Sub	1006	(A)₁₅=0.3131	delA=0.6869
1000Genomes	South Asian	Sub	978	(A)₁₅=0.348	delA=0.652
1000Genomes	American	Sub	694	(A)₁₅=0.334	delA=0.666
Allele Frequency Aggregator	Total	Global	810	(A)₁₅=1.000	delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000
Allele Frequency Aggregator	European	Sub	636	(A)₁₅=1.000	delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000
Allele Frequency Aggregator	African	Sub	92	(A)₁₅=1.00	delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00
Allele Frequency Aggregator	Latin American 2	Sub	38	(A)₁₅=1.00	delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00
Allele Frequency Aggregator	Other	Sub	32	(A)₁₅=1.00	delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00
Allele Frequency Aggregator	Asian	Sub	6	(A)₁₅=1.0	delAAA=0.0, delAA=0.0, delA=0.0, dupA=0.0, dupAA=0.0
Allele Frequency Aggregator	Latin American 1	Sub	4	(A)₁₅=1.0	delAAA=0.0, delAA=0.0, delA=0.0, dupA=0.0, dupAA=0.0
Allele Frequency Aggregator	South Asian	Sub	2	(A)₁₅=1.0	delAAA=0.0, delAA=0.0, delA=0.0, dupA=0.0, dupAA=0.0

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 11	NC_000011.10:g.126226963_126226965del
GRCh38.p14 chr 11	NC_000011.10:g.126226964_126226965del
GRCh38.p14 chr 11	NC_000011.10:g.126226965del
GRCh38.p14 chr 11	NC_000011.10:g.126226965dup
GRCh38.p14 chr 11	NC_000011.10:g.126226964_126226965dup
GRCh37.p13 chr 11	NC_000011.9:g.126096858_126096860del
GRCh37.p13 chr 11	NC_000011.9:g.126096859_126096860del
GRCh37.p13 chr 11	NC_000011.9:g.126096860del
GRCh37.p13 chr 11	NC_000011.9:g.126096860dup
GRCh37.p13 chr 11	NC_000011.9:g.126096859_126096860dup
FAM118B RefSeqGene	NG_017156.1:g.20240_20242del
FAM118B RefSeqGene	NG_017156.1:g.20241_20242del
FAM118B RefSeqGene	NG_017156.1:g.20242del
FAM118B RefSeqGene	NG_017156.1:g.20242dup
FAM118B RefSeqGene	NG_017156.1:g.20241_20242dup

Gene: FAM118B, family with sequence similarity 118 member B (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
FAM118B transcript variant 2	NM_001330446.1:c.-76-2262… NM_001330446.1:c.-76-2262_-76-2260del	N/A	Intron Variant
FAM118B transcript variant 1	NM_024556.4:c.-76-2262_-7… NM_024556.4:c.-76-2262_-76-2260del	N/A	Intron Variant
FAM118B transcript variant X1	XM_011542977.4:c.-7-8032_… XM_011542977.4:c.-7-8032_-7-8030del	N/A	Intron Variant
FAM118B transcript variant X3	XM_011542978.4:c.-76-2262… XM_011542978.4:c.-76-2262_-76-2260del	N/A	Intron Variant
FAM118B transcript variant X2	XM_017018285.3:c.-7-8032_… XM_017018285.3:c.-7-8032_-7-8030del	N/A	Intron Variant
FAM118B transcript variant X4	XM_047427584.1:c.	N/A	Genic Upstream 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)₁₅=	delAAA	delAA	delA	dupA	dupAA
GRCh38.p14 chr 11	NC_000011.10:g.126226951_126226965=	NC_000011.10:g.126226963_126226965del	NC_000011.10:g.126226964_126226965del	NC_000011.10:g.126226965del	NC_000011.10:g.126226965dup	NC_000011.10:g.126226964_126226965dup
GRCh37.p13 chr 11	NC_000011.9:g.126096846_126096860=	NC_000011.9:g.126096858_126096860del	NC_000011.9:g.126096859_126096860del	NC_000011.9:g.126096860del	NC_000011.9:g.126096860dup	NC_000011.9:g.126096859_126096860dup
FAM118B RefSeqGene	NG_017156.1:g.20228_20242=	NG_017156.1:g.20240_20242del	NG_017156.1:g.20241_20242del	NG_017156.1:g.20242del	NG_017156.1:g.20242dup	NG_017156.1:g.20241_20242dup
FAM118B transcript variant 2	NM_001330446.1:c.-76-2274=	NM_001330446.1:c.-76-2262_-76-2260del	NM_001330446.1:c.-76-2261_-76-2260del	NM_001330446.1:c.-76-2260del	NM_001330446.1:c.-76-2260dup	NM_001330446.1:c.-76-2261_-76-2260dup
FAM118B transcript variant 1	NM_024556.3:c.-76-2274=	NM_024556.3:c.-76-2262_-76-2260del	NM_024556.3:c.-76-2261_-76-2260del	NM_024556.3:c.-76-2260del	NM_024556.3:c.-76-2260dup	NM_024556.3:c.-76-2261_-76-2260dup
FAM118B transcript variant 1	NM_024556.4:c.-76-2274=	NM_024556.4:c.-76-2262_-76-2260del	NM_024556.4:c.-76-2261_-76-2260del	NM_024556.4:c.-76-2260del	NM_024556.4:c.-76-2260dup	NM_024556.4:c.-76-2261_-76-2260dup
FAM118B transcript variant X1	XM_005271665.1:c.-76-2274=	XM_005271665.1:c.-76-2262_-76-2260del	XM_005271665.1:c.-76-2261_-76-2260del	XM_005271665.1:c.-76-2260del	XM_005271665.1:c.-76-2260dup	XM_005271665.1:c.-76-2261_-76-2260dup
FAM118B transcript variant X2	XM_005271666.1:c.-76-2274=	XM_005271666.1:c.-76-2262_-76-2260del	XM_005271666.1:c.-76-2261_-76-2260del	XM_005271666.1:c.-76-2260del	XM_005271666.1:c.-76-2260dup	XM_005271666.1:c.-76-2261_-76-2260dup
FAM118B transcript variant X1	XM_011542977.4:c.-7-8044=	XM_011542977.4:c.-7-8032_-7-8030del	XM_011542977.4:c.-7-8031_-7-8030del	XM_011542977.4:c.-7-8030del	XM_011542977.4:c.-7-8030dup	XM_011542977.4:c.-7-8031_-7-8030dup
FAM118B transcript variant X3	XM_011542978.4:c.-76-2274=	XM_011542978.4:c.-76-2262_-76-2260del	XM_011542978.4:c.-76-2261_-76-2260del	XM_011542978.4:c.-76-2260del	XM_011542978.4:c.-76-2260dup	XM_011542978.4:c.-76-2261_-76-2260dup
FAM118B transcript variant X2	XM_017018285.3:c.-7-8044=	XM_017018285.3:c.-7-8032_-7-8030del	XM_017018285.3:c.-7-8031_-7-8030del	XM_017018285.3:c.-7-8030del	XM_017018285.3:c.-7-8030dup	XM_017018285.3:c.-7-8031_-7-8030dup

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#.

46 SubSNP, 15 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	HUMANGENOME_JCVI	ss95583489	Feb 13, 2009 (137)
2	GMI	ss289102582	May 04, 2012 (137)
3	GMI	ss289102583	May 04, 2012 (137)
4	PJP	ss294728567	May 09, 2011 (137)
5	SSMP	ss664030915	Apr 01, 2015 (144)
6	SSIP	ss947287889	Aug 21, 2014 (142)
7	1000GENOMES	ss1371649737	Aug 21, 2014 (142)
8	HAMMER_LAB	ss1807047277	Sep 08, 2015 (146)
9	SYSTEMSBIOZJU	ss2627958854	Nov 08, 2017 (151)
10	SWEGEN	ss3008953002	Nov 08, 2017 (151)
11	MCHAISSO	ss3063712407	Nov 08, 2017 (151)
12	MCHAISSO	ss3064539391	Nov 08, 2017 (151)
13	MCHAISSO	ss3065454734	Nov 08, 2017 (151)
14	BIOINF_KMB_FNS_UNIBA	ss3645226916	Oct 12, 2018 (152)
15	EVA_DECODE	ss3692810867	Jul 13, 2019 (153)
16	EVA_DECODE	ss3692810868	Jul 13, 2019 (153)
17	EVA_DECODE	ss3692810869	Jul 13, 2019 (153)
18	EVA_DECODE	ss3692810870	Jul 13, 2019 (153)
19	ACPOP	ss3738634444	Jul 13, 2019 (153)
20	ACPOP	ss3738634445	Jul 13, 2019 (153)
21	PACBIO	ss3787097524	Jul 13, 2019 (153)
22	PACBIO	ss3792217218	Jul 13, 2019 (153)
23	PACBIO	ss3797099740	Jul 13, 2019 (153)
24	KHV_HUMAN_GENOMES	ss3815272484	Jul 13, 2019 (153)
25	EVA	ss3832893712	Apr 26, 2020 (154)
26	EVA	ss3840009424	Apr 26, 2020 (154)
27	EVA	ss3845491833	Apr 26, 2020 (154)
28	GNOMAD	ss4244418303	Apr 26, 2021 (155)
29	GNOMAD	ss4244418304	Apr 26, 2021 (155)
30	GNOMAD	ss4244418305	Apr 26, 2021 (155)
31	GNOMAD	ss4244418306	Apr 26, 2021 (155)
32	TOMMO_GENOMICS	ss5204372841	Apr 26, 2021 (155)
33	TOMMO_GENOMICS	ss5204372842	Apr 26, 2021 (155)
34	TOMMO_GENOMICS	ss5204372843	Apr 26, 2021 (155)
35	1000G_HIGH_COVERAGE	ss5289273945	Oct 16, 2022 (156)
36	1000G_HIGH_COVERAGE	ss5289273946	Oct 16, 2022 (156)
37	1000G_HIGH_COVERAGE	ss5289273947	Oct 16, 2022 (156)
38	HUGCELL_USP	ss5484225485	Oct 16, 2022 (156)
39	HUGCELL_USP	ss5484225486	Oct 16, 2022 (156)
40	HUGCELL_USP	ss5484225487	Oct 16, 2022 (156)
41	TOMMO_GENOMICS	ss5752962301	Oct 16, 2022 (156)
42	TOMMO_GENOMICS	ss5752962302	Oct 16, 2022 (156)
43	TOMMO_GENOMICS	ss5752962303	Oct 16, 2022 (156)
44	EVA	ss5837376805	Oct 16, 2022 (156)
45	EVA	ss5837376806	Oct 16, 2022 (156)
46	EVA	ss5922092896	Oct 16, 2022 (156)
47	1000Genomes	NC_000011.9 - 126096846	Oct 12, 2018 (152)
48	gnomAD - Genomes Submission ignored due to conflicting rows: Row 395009157 (NC_000011.10:126226950::A 748/111250) Row 395009158 (NC_000011.10:126226950::AA 0/111286) Row 395009159 (NC_000011.10:126226950:A: 78600/111170)...	-	Apr 26, 2021 (155)
49	gnomAD - Genomes Submission ignored due to conflicting rows: Row 395009157 (NC_000011.10:126226950::A 748/111250) Row 395009158 (NC_000011.10:126226950::AA 0/111286) Row 395009159 (NC_000011.10:126226950:A: 78600/111170)...	-	Apr 26, 2021 (155)
50	gnomAD - Genomes Submission ignored due to conflicting rows: Row 395009157 (NC_000011.10:126226950::A 748/111250) Row 395009158 (NC_000011.10:126226950::AA 0/111286) Row 395009159 (NC_000011.10:126226950:A: 78600/111170)...	-	Apr 26, 2021 (155)
51	gnomAD - Genomes Submission ignored due to conflicting rows: Row 395009157 (NC_000011.10:126226950::A 748/111250) Row 395009158 (NC_000011.10:126226950::AA 0/111286) Row 395009159 (NC_000011.10:126226950:A: 78600/111170)...	-	Apr 26, 2021 (155)
52	gnomAD - Genomes Submission ignored due to conflicting rows: Row 395009157 (NC_000011.10:126226950::A 748/111250) Row 395009158 (NC_000011.10:126226950::AA 0/111286) Row 395009159 (NC_000011.10:126226950:A: 78600/111170)...	-	Apr 26, 2021 (155)
53	Northern Sweden Submission ignored due to conflicting rows: Row 11919309 (NC_000011.9:126096845:A: 352/504) Row 11919310 (NC_000011.9:126096845:AA: 6/504)	-	Jul 13, 2019 (153)
54	Northern Sweden Submission ignored due to conflicting rows: Row 11919309 (NC_000011.9:126096845:A: 352/504) Row 11919310 (NC_000011.9:126096845:AA: 6/504)	-	Jul 13, 2019 (153)
55	8.3KJPN Submission ignored due to conflicting rows: Row 62342148 (NC_000011.9:126096845:A: 12675/16698) Row 62342149 (NC_000011.9:126096845:AA: 17/16698) Row 62342150 (NC_000011.9:126096845::A 2/16698)	-	Apr 26, 2021 (155)
56	8.3KJPN Submission ignored due to conflicting rows: Row 62342148 (NC_000011.9:126096845:A: 12675/16698) Row 62342149 (NC_000011.9:126096845:AA: 17/16698) Row 62342150 (NC_000011.9:126096845::A 2/16698)	-	Apr 26, 2021 (155)
57	8.3KJPN Submission ignored due to conflicting rows: Row 62342148 (NC_000011.9:126096845:A: 12675/16698) Row 62342149 (NC_000011.9:126096845:AA: 17/16698) Row 62342150 (NC_000011.9:126096845::A 2/16698)	-	Apr 26, 2021 (155)
58	14KJPN Submission ignored due to conflicting rows: Row 86799405 (NC_000011.10:126226950:A: 21527/28258) Row 86799406 (NC_000011.10:126226950:AA: 19/28258) Row 86799407 (NC_000011.10:126226950::A 3/28258)	-	Oct 16, 2022 (156)
59	14KJPN Submission ignored due to conflicting rows: Row 86799405 (NC_000011.10:126226950:A: 21527/28258) Row 86799406 (NC_000011.10:126226950:AA: 19/28258) Row 86799407 (NC_000011.10:126226950::A 3/28258)	-	Oct 16, 2022 (156)
60	14KJPN Submission ignored due to conflicting rows: Row 86799405 (NC_000011.10:126226950:A: 21527/28258) Row 86799406 (NC_000011.10:126226950:AA: 19/28258) Row 86799407 (NC_000011.10:126226950::A 3/28258)	-	Oct 16, 2022 (156)
61	ALFA	NC_000011.10 - 126226951	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)
rs35985102	May 23, 2006 (127)
rs71048773	May 11, 2012 (137)
rs72365925	May 11, 2012 (137)
rs72398687	May 11, 2012 (137)
rs202212875	May 11, 2012 (137)
rs376041111	May 13, 2013 (138)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss3692810870, ss4244418306	NC_000011.10:126226950:AAA:	NC_000011.10:126226950:AAAAAAAAAAA… NC_000011.10:126226950:AAAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
10860741531	NC_000011.10:126226950:AAAAAAAAAAA… NC_000011.10:126226950:AAAAAAAAAAAAAAA:AAAAAAAAAAAA	NC_000011.10:126226950:AAAAAAAAAAA… NC_000011.10:126226950:AAAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
ss289102583	NC_000011.8:125602055:AA:	NC_000011.10:126226950:AAAAAAAAAAA… NC_000011.10:126226950:AAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss3008953002, ss3738634445, ss5204372842, ss5837376806	NC_000011.9:126096845:AA:	NC_000011.10:126226950:AAAAAAAAAAA… NC_000011.10:126226950:AAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss4244418305, ss5289273946, ss5484225486, ss5752962302	NC_000011.10:126226950:AA:	NC_000011.10:126226950:AAAAAAAAAAA… NC_000011.10:126226950:AAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
10860741531	NC_000011.10:126226950:AAAAAAAAAAA… NC_000011.10:126226950:AAAAAAAAAAAAAAA:AAAAAAAAAAAAA	NC_000011.10:126226950:AAAAAAAAAAA… NC_000011.10:126226950:AAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss3692810869	NC_000011.10:126226951:AA:	NC_000011.10:126226950:AAAAAAAAAAA… NC_000011.10:126226950:AAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss289102582	NC_000011.8:125602055:A:	NC_000011.10:126226950:AAAAAAAAAAA… NC_000011.10:126226950:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss294728567	NC_000011.8:125602069:A:	NC_000011.10:126226950:AAAAAAAAAAA… NC_000011.10:126226950:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
55992046, ss664030915, ss1371649737, ss1807047277, ss2627958854, ss3738634444, ss3787097524, ss3792217218, ss3797099740, ss3832893712, ss3840009424, ss5204372841, ss5837376805	NC_000011.9:126096845:A:	NC_000011.10:126226950:AAAAAAAAAAA… NC_000011.10:126226950:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss947287889	NC_000011.9:126096846:A:	NC_000011.10:126226950:AAAAAAAAAAA… NC_000011.10:126226950:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss3063712407, ss3064539391, ss3065454734, ss3645226916, ss3815272484, ss3845491833, ss5289273945, ss5484225485, ss5752962301, ss5922092896	NC_000011.10:126226950:A:	NC_000011.10:126226950:AAAAAAAAAAA… NC_000011.10:126226950:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
10860741531	NC_000011.10:126226950:AAAAAAAAAAA… NC_000011.10:126226950:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	NC_000011.10:126226950:AAAAAAAAAAA… NC_000011.10:126226950:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss3692810868	NC_000011.10:126226952:A:	NC_000011.10:126226950:AAAAAAAAAAA… NC_000011.10:126226950:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss95583489	NT_033899.8:29659275:A:	NC_000011.10:126226950:AAAAAAAAAAA… NC_000011.10:126226950:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss5204372843	NC_000011.9:126096845::A	NC_000011.10:126226950:AAAAAAAAAAA… NC_000011.10:126226950:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss4244418303, ss5289273947, ss5484225487, ss5752962303	NC_000011.10:126226950::A	NC_000011.10:126226950:AAAAAAAAAAA… NC_000011.10:126226950:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
10860741531	NC_000011.10:126226950:AAAAAAAAAAA… NC_000011.10:126226950:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	NC_000011.10:126226950:AAAAAAAAAAA… NC_000011.10:126226950:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss3692810867	NC_000011.10:126226953::A	NC_000011.10:126226950:AAAAAAAAAAA… NC_000011.10:126226950:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss4244418304	NC_000011.10:126226950::AA	NC_000011.10:126226950:AAAAAAAAAAA… NC_000011.10:126226950:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
10860741531	NC_000011.10:126226950:AAAAAAAAAAA… NC_000011.10:126226950:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	NC_000011.10:126226950:AAAAAAAAAAA… NC_000011.10:126226950:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(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 rs11320787

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

rs11320787