Name: rs11318208
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.

rs11318208

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr11:4914545-4914552 (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: delCC / delC / dupC / dupCC
Variation Type: Indel Insertion and Deletion
Frequency: delC=0.1657 (1645/9928, ALFA)
dupC=0.1000 (501/5008, 1000G)
delC=0.3770 (1600/4244, Estonian)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: MMP26 : Intron Variant
OR51G2 : 3 Prime UTR 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	9928	CCCCCCCC=0.8222	CCCCCC=0.0000, CCCCCCC=0.1657, CCCCCCCCC=0.0121, CCCCCCCCCC=0.0000	0.734985	0.063983	0.201032	32
European	Sub	7744	CCCCCCCC=0.7723	CCCCCC=0.0000, CCCCCCC=0.2123, CCCCCCCCC=0.0154, CCCCCCCCCC=0.0000	0.657965	0.082579	0.259457	32
African	Sub	1468	CCCCCCCC=1.0000	CCCCCC=0.0000, CCCCCCC=0.0000, CCCCCCCCC=0.0000, CCCCCCCCCC=0.0000	1.0	0.0	0.0	N/A
African Others	Sub	70	CCCCCCCC=1.00	CCCCCC=0.00, CCCCCCC=0.00, CCCCCCCCC=0.00, CCCCCCCCCC=0.00	1.0	0.0	0.0	N/A
African American	Sub	1398	CCCCCCCC=1.0000	CCCCCC=0.0000, CCCCCCC=0.0000, CCCCCCCCC=0.0000, CCCCCCCCCC=0.0000	1.0	0.0	0.0	N/A
Asian	Sub	52	CCCCCCCC=1.00	CCCCCC=0.00, CCCCCCC=0.00, CCCCCCCCC=0.00, CCCCCCCCCC=0.00	1.0	0.0	0.0	N/A
East Asian	Sub	42	CCCCCCCC=1.00	CCCCCC=0.00, CCCCCCC=0.00, CCCCCCCCC=0.00, CCCCCCCCCC=0.00	1.0	0.0	0.0	N/A
Other Asian	Sub	10	CCCCCCCC=1.0	CCCCCC=0.0, CCCCCCC=0.0, CCCCCCCCC=0.0, CCCCCCCCCC=0.0	1.0	0.0	0.0	N/A
Latin American 1	Sub	72	CCCCCCCC=1.00	CCCCCC=0.00, CCCCCCC=0.00, CCCCCCCCC=0.00, CCCCCCCCCC=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	344	CCCCCCCC=1.000	CCCCCC=0.000, CCCCCCC=0.000, CCCCCCCCC=0.000, CCCCCCCCCC=0.000	1.0	0.0	0.0	N/A
South Asian	Sub	24	CCCCCCCC=1.00	CCCCCC=0.00, CCCCCCC=0.00, CCCCCCCCC=0.00, CCCCCCCCCC=0.00	1.0	0.0	0.0	N/A
Other	Sub	224	CCCCCCCC=0.991	CCCCCC=0.000, CCCCCCC=0.004, CCCCCCCCC=0.004, CCCCCCCCCC=0.000	1.0	0.0	0.0	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
Allele Frequency Aggregator	Total	Global	9928	(C)₈=0.8222	delCC=0.0000, delC=0.1657, dupC=0.0121, dupCC=0.0000
Allele Frequency Aggregator	European	Sub	7744	(C)₈=0.7723	delCC=0.0000, delC=0.2123, dupC=0.0154, dupCC=0.0000
Allele Frequency Aggregator	African	Sub	1468	(C)₈=1.0000	delCC=0.0000, delC=0.0000, dupC=0.0000, dupCC=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	344	(C)₈=1.000	delCC=0.000, delC=0.000, dupC=0.000, dupCC=0.000
Allele Frequency Aggregator	Other	Sub	224	(C)₈=0.991	delCC=0.000, delC=0.004, dupC=0.004, dupCC=0.000
Allele Frequency Aggregator	Latin American 1	Sub	72	(C)₈=1.00	delCC=0.00, delC=0.00, dupC=0.00, dupCC=0.00
Allele Frequency Aggregator	Asian	Sub	52	(C)₈=1.00	delCC=0.00, delC=0.00, dupC=0.00, dupCC=0.00
Allele Frequency Aggregator	South Asian	Sub	24	(C)₈=1.00	delCC=0.00, delC=0.00, dupC=0.00, dupCC=0.00
1000Genomes	Global	Study-wide	5008	- No frequency provided	dupC=0.1000
1000Genomes	African	Sub	1322	- No frequency provided	dupC=0.1346
1000Genomes	East Asian	Sub	1008	- No frequency provided	dupC=0.0605
1000Genomes	Europe	Sub	1006	- No frequency provided	dupC=0.0417
1000Genomes	South Asian	Sub	978	- No frequency provided	dupC=0.197
1000Genomes	American	Sub	694	- No frequency provided	dupC=0.039
Genetic variation in the Estonian population	Estonian	Study-wide	4244	(C)₈=0.6230	delC=0.3770

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.4914551_4914552del
GRCh38.p14 chr 11	NC_000011.10:g.4914552del
GRCh38.p14 chr 11	NC_000011.10:g.4914552dup
GRCh38.p14 chr 11	NC_000011.10:g.4914551_4914552dup
GRCh37.p13 chr 11	NC_000011.9:g.4935781_4935782del
GRCh37.p13 chr 11	NC_000011.9:g.4935782del
GRCh37.p13 chr 11	NC_000011.9:g.4935782dup
GRCh37.p13 chr 11	NC_000011.9:g.4935781_4935782dup

Gene: MMP26, matrix metallopeptidase 26 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
MMP26 transcript variant 2	NM_001384608.1:c.-152-737… NM_001384608.1:c.-152-73719_-152-73718del	N/A	Intron Variant
MMP26 transcript variant 1	NM_021801.5:c.-144-73517_… NM_021801.5:c.-144-73517_-144-73516del	N/A	Intron Variant
MMP26 transcript variant X1	XM_011520219.3:c.	N/A	Genic Upstream Transcript Variant

Gene: OR51G2, olfactory receptor family 51 subfamily G member 2 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
OR51G2 transcript	NM_001005238.2:c.167_17… NM_001005238.2:c.167_174=	N/A	3 Prime UTR 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	(C)₈=	delCC	delC	dupC	dupCC
GRCh38.p14 chr 11	NC_000011.10:g.4914545_4914552=	NC_000011.10:g.4914551_4914552del	NC_000011.10:g.4914552del	NC_000011.10:g.4914552dup	NC_000011.10:g.4914551_4914552dup
GRCh37.p13 chr 11	NC_000011.9:g.4935775_4935782=	NC_000011.9:g.4935781_4935782del	NC_000011.9:g.4935782del	NC_000011.9:g.4935782dup	NC_000011.9:g.4935781_4935782dup
OR51G2 transcript	NM_001005238.2:c.167_174=	NM_001005238.2:c.173_174del	NM_001005238.2:c.*174del	NM_001005238.2:c.*174dup	NM_001005238.2:c.173_174dup
MMP26 transcript variant 2	NM_001384608.1:c.-152-73725=	NM_001384608.1:c.-152-73719_-152-73718del	NM_001384608.1:c.-152-73718del	NM_001384608.1:c.-152-73718dup	NM_001384608.1:c.-152-73719_-152-73718dup
MMP26 transcript variant 1	NM_021801.5:c.-144-73523=	NM_021801.5:c.-144-73517_-144-73516del	NM_021801.5:c.-144-73516del	NM_021801.5:c.-144-73516dup	NM_021801.5:c.-144-73517_-144-73516dup

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#.

60 SubSNP, 18 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	ABI	ss39993553	Dec 03, 2013 (138)
2	HUMANGENOME_JCVI	ss95558979	Feb 05, 2009 (130)
3	BUSHMAN	ss193215573	Jul 04, 2010 (137)
4	GMI	ss287869105	May 09, 2011 (137)
5	GMI	ss289050030	May 04, 2012 (137)
6	PJP	ss294686401	May 09, 2011 (137)
7	PJP	ss294686402	May 09, 2011 (134)
8	1000GENOMES	ss327303511	May 09, 2011 (137)
9	1000GENOMES	ss327387460	May 09, 2011 (137)
10	1000GENOMES	ss327784956	Jan 10, 2018 (151)
11	LUNTER	ss552094905	Apr 25, 2013 (138)
12	LUNTER	ss552343094	Apr 25, 2013 (138)
13	LUNTER	ss553435815	Apr 25, 2013 (138)
14	TISHKOFF	ss554561195	Apr 25, 2013 (138)
15	SSMP	ss664056500	Apr 01, 2015 (144)
16	BILGI_BIOE	ss666522703	Apr 25, 2013 (138)
17	1000GENOMES	ss1370448374	Aug 21, 2014 (142)
18	EVA_UK10K_ALSPAC	ss1706978988	Apr 01, 2015 (144)
19	EVA_UK10K_TWINSUK	ss1706979555	Apr 01, 2015 (144)
20	EVA_UK10K_ALSPAC	ss1710498122	Oct 12, 2018 (152)
21	EVA_UK10K_TWINSUK	ss1710498132	Oct 12, 2018 (152)
22	HAMMER_LAB	ss1806669687	Sep 08, 2015 (146)
23	TMC_SNPDB	ss1997038420	Oct 12, 2018 (152)
24	SYSTEMSBIOZJU	ss2627718449	Nov 08, 2017 (151)
25	SWEGEN	ss3007518202	Jan 10, 2018 (151)
26	BIOINF_KMB_FNS_UNIBA	ss3645175420	Oct 12, 2018 (152)
27	URBANLAB	ss3649520051	Oct 12, 2018 (152)
28	EGCUT_WGS	ss3674914441	Jul 13, 2019 (153)
29	EVA_DECODE	ss3691121932	Jul 13, 2019 (153)
30	EVA_DECODE	ss3691121933	Jul 13, 2019 (153)
31	EVA_DECODE	ss3691121934	Jul 13, 2019 (153)
32	ACPOP	ss3737876066	Jul 13, 2019 (153)
33	ACPOP	ss3737876067	Jul 13, 2019 (153)
34	PACBIO	ss3786850480	Jul 13, 2019 (153)
35	PACBIO	ss3792005924	Jul 13, 2019 (153)
36	PACBIO	ss3796887937	Jul 13, 2019 (153)
37	KHV_HUMAN_GENOMES	ss3814231509	Jul 13, 2019 (153)
38	EVA	ss3832449980	Apr 26, 2020 (154)
39	EVA	ss3839769297	Apr 26, 2020 (154)
40	EVA	ss3845245215	Apr 26, 2020 (154)
41	GNOMAD	ss4229262488	Apr 26, 2021 (155)
42	GNOMAD	ss4229262489	Apr 26, 2021 (155)
43	GNOMAD	ss4229262492	Apr 26, 2021 (155)
44	TOMMO_GENOMICS	ss5200477905	Apr 26, 2021 (155)
45	TOMMO_GENOMICS	ss5200477906	Apr 26, 2021 (155)
46	TOMMO_GENOMICS	ss5200477907	Apr 26, 2021 (155)
47	EVA	ss5237212481	Apr 26, 2021 (155)
48	EVA	ss5237212482	Apr 26, 2021 (155)
49	1000G_HIGH_COVERAGE	ss5286241121	Oct 16, 2022 (156)
50	1000G_HIGH_COVERAGE	ss5286241122	Oct 16, 2022 (156)
51	HUGCELL_USP	ss5481562304	Oct 16, 2022 (156)
52	HUGCELL_USP	ss5481562305	Oct 16, 2022 (156)
53	EVA	ss5624016739	Oct 16, 2022 (156)
54	TOMMO_GENOMICS	ss5747174932	Oct 16, 2022 (156)
55	TOMMO_GENOMICS	ss5747174933	Oct 16, 2022 (156)
56	TOMMO_GENOMICS	ss5747174934	Oct 16, 2022 (156)
57	EVA	ss5800165369	Oct 16, 2022 (156)
58	EVA	ss5836196573	Oct 16, 2022 (156)
59	EVA	ss5836196574	Oct 16, 2022 (156)
60	EVA	ss5980656452	Oct 16, 2022 (156)
61	1000Genomes	NC_000011.9 - 4935775	Oct 12, 2018 (152)
62	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 29107106 (NC_000011.9:4935774:C: 1214/3854) Row 29107107 (NC_000011.9:4935774::C 145/3854)	-	Oct 12, 2018 (152)
63	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 29107106 (NC_000011.9:4935774:C: 1214/3854) Row 29107107 (NC_000011.9:4935774::C 145/3854)	-	Oct 12, 2018 (152)
64	Genetic variation in the Estonian population	NC_000011.9 - 4935775	Oct 12, 2018 (152)
65	gnomAD - Genomes Submission ignored due to conflicting rows: Row 370044269 (NC_000011.10:4914544::C 9827/138778) Row 370044270 (NC_000011.10:4914544::CC 29/138832) Row 370044273 (NC_000011.10:4914544:C: 36261/138774)	-	Apr 26, 2021 (155)
66	gnomAD - Genomes Submission ignored due to conflicting rows: Row 370044269 (NC_000011.10:4914544::C 9827/138778) Row 370044270 (NC_000011.10:4914544::CC 29/138832) Row 370044273 (NC_000011.10:4914544:C: 36261/138774)	-	Apr 26, 2021 (155)
67	gnomAD - Genomes Submission ignored due to conflicting rows: Row 370044269 (NC_000011.10:4914544::C 9827/138778) Row 370044270 (NC_000011.10:4914544::CC 29/138832) Row 370044273 (NC_000011.10:4914544:C: 36261/138774)	-	Apr 26, 2021 (155)
68	Northern Sweden Submission ignored due to conflicting rows: Row 11160931 (NC_000011.9:4935774:C: 152/600) Row 11160932 (NC_000011.9:4935774::C 36/600)	-	Jul 13, 2019 (153)
69	Northern Sweden Submission ignored due to conflicting rows: Row 11160931 (NC_000011.9:4935774:C: 152/600) Row 11160932 (NC_000011.9:4935774::C 36/600)	-	Jul 13, 2019 (153)
70	8.3KJPN Submission ignored due to conflicting rows: Row 58447212 (NC_000011.9:4935774::C 1721/16758) Row 58447213 (NC_000011.9:4935774:C: 4554/16758) Row 58447214 (NC_000011.9:4935774::CC 4/16758)	-	Apr 26, 2021 (155)
71	8.3KJPN Submission ignored due to conflicting rows: Row 58447212 (NC_000011.9:4935774::C 1721/16758) Row 58447213 (NC_000011.9:4935774:C: 4554/16758) Row 58447214 (NC_000011.9:4935774::CC 4/16758)	-	Apr 26, 2021 (155)
72	8.3KJPN Submission ignored due to conflicting rows: Row 58447212 (NC_000011.9:4935774::C 1721/16758) Row 58447213 (NC_000011.9:4935774:C: 4554/16758) Row 58447214 (NC_000011.9:4935774::CC 4/16758)	-	Apr 26, 2021 (155)
73	14KJPN Submission ignored due to conflicting rows: Row 81012036 (NC_000011.10:4914544:C: 7647/28258) Row 81012037 (NC_000011.10:4914544::C 2941/28258) Row 81012038 (NC_000011.10:4914544::CC 6/28258)	-	Oct 16, 2022 (156)
74	14KJPN Submission ignored due to conflicting rows: Row 81012036 (NC_000011.10:4914544:C: 7647/28258) Row 81012037 (NC_000011.10:4914544::C 2941/28258) Row 81012038 (NC_000011.10:4914544::CC 6/28258)	-	Oct 16, 2022 (156)
75	14KJPN Submission ignored due to conflicting rows: Row 81012036 (NC_000011.10:4914544:C: 7647/28258) Row 81012037 (NC_000011.10:4914544::C 2941/28258) Row 81012038 (NC_000011.10:4914544::CC 6/28258)	-	Oct 16, 2022 (156)
76	UK 10K study - Twins Submission ignored due to conflicting rows: Row 29107106 (NC_000011.9:4935774:C: 1190/3708) Row 29107107 (NC_000011.9:4935774::C 156/3708)	-	Oct 12, 2018 (152)
77	UK 10K study - Twins Submission ignored due to conflicting rows: Row 29107106 (NC_000011.9:4935774:C: 1190/3708) Row 29107107 (NC_000011.9:4935774::C 156/3708)	-	Oct 12, 2018 (152)
78	ALFA	NC_000011.10 - 4914545	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)
rs112141503	May 11, 2012 (137)
rs140172846	May 04, 2012 (137)
rs368061208	May 13, 2013 (138)
rs371732921	May 15, 2013 (138)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
6176605454	NC_000011.10:4914544:CCCCCCCC:CCCC… NC_000011.10:4914544:CCCCCCCC:CCCCCC	NC_000011.10:4914544:CCCCCCCC:CCCC… NC_000011.10:4914544:CCCCCCCC:CCCCCC	(self)
ss289050030, ss294686401, ss327303511, ss327387460, ss552094905, ss553435815	NC_000011.8:4892350:C:	NC_000011.10:4914544:CCCCCCCC:CCCC… NC_000011.10:4914544:CCCCCCCC:CCCCCCC	(self)
ss294686402	NC_000011.8:4892357:C:	NC_000011.10:4914544:CCCCCCCC:CCCC… NC_000011.10:4914544:CCCCCCCC:CCCCCCC	(self)
20652689, ss664056500, ss666522703, ss1706978988, ss1706979555, ss1806669687, ss3007518202, ss3674914441, ss3737876066, ss3786850480, ss3792005924, ss3796887937, ss3832449980, ss3839769297, ss5200477906, ss5624016739, ss5800165369, ss5836196573, ss5980656452	NC_000011.9:4935774:C:	NC_000011.10:4914544:CCCCCCCC:CCCC… NC_000011.10:4914544:CCCCCCCC:CCCCCCC	(self)
ss554561195	NC_000011.9:4935781:C:	NC_000011.10:4914544:CCCCCCCC:CCCC… NC_000011.10:4914544:CCCCCCCC:CCCCCCC	(self)
ss3645175420, ss3649520051, ss3691121934, ss3845245215, ss4229262492, ss5237212481, ss5286241121, ss5481562304, ss5747174932	NC_000011.10:4914544:C:	NC_000011.10:4914544:CCCCCCCC:CCCC… NC_000011.10:4914544:CCCCCCCC:CCCCCCC	(self)
6176605454	NC_000011.10:4914544:CCCCCCCC:CCCC… NC_000011.10:4914544:CCCCCCCC:CCCCCCC	NC_000011.10:4914544:CCCCCCCC:CCCC… NC_000011.10:4914544:CCCCCCCC:CCCCCCC	(self)
ss287869105	NT_009237.18:4875774:C:	NC_000011.10:4914544:CCCCCCCC:CCCC… NC_000011.10:4914544:CCCCCCCC:CCCCCCC	(self)
ss39993553, ss95558979	NT_009237.18:4875781:C:	NC_000011.10:4914544:CCCCCCCC:CCCC… NC_000011.10:4914544:CCCCCCCC:CCCCCCC	(self)
ss193215573	NT_009237.19:4854544:C:	NC_000011.10:4914544:CCCCCCCC:CCCC… NC_000011.10:4914544:CCCCCCCC:CCCCCCC	(self)
ss327784956, ss552343094	NC_000011.8:4892350::C	NC_000011.10:4914544:CCCCCCCC:CCCC… NC_000011.10:4914544:CCCCCCCC:CCCCCCCCC	(self)
52405076, ss1370448374, ss2627718449, ss3737876067, ss5200477905, ss5836196574	NC_000011.9:4935774::C	NC_000011.10:4914544:CCCCCCCC:CCCC… NC_000011.10:4914544:CCCCCCCC:CCCCCCCCC	(self)
ss1710498122, ss1710498132, ss1997038420	NC_000011.9:4935775::C	NC_000011.10:4914544:CCCCCCCC:CCCC… NC_000011.10:4914544:CCCCCCCC:CCCCCCCCC	(self)
ss3814231509, ss4229262488, ss5286241122, ss5481562305, ss5747174933	NC_000011.10:4914544::C	NC_000011.10:4914544:CCCCCCCC:CCCC… NC_000011.10:4914544:CCCCCCCC:CCCCCCCCC	(self)
6176605454	NC_000011.10:4914544:CCCCCCCC:CCCC… NC_000011.10:4914544:CCCCCCCC:CCCCCCCCC	NC_000011.10:4914544:CCCCCCCC:CCCC… NC_000011.10:4914544:CCCCCCCC:CCCCCCCCC	(self)
ss3691121933, ss5237212482	NC_000011.10:4914545::C	NC_000011.10:4914544:CCCCCCCC:CCCC… NC_000011.10:4914544:CCCCCCCC:CCCCCCCCC	(self)
ss5200477907	NC_000011.9:4935774::CC	NC_000011.10:4914544:CCCCCCCC:CCCC… NC_000011.10:4914544:CCCCCCCC:CCCCCCCCCC	(self)
ss4229262489, ss5747174934	NC_000011.10:4914544::CC	NC_000011.10:4914544:CCCCCCCC:CCCC… NC_000011.10:4914544:CCCCCCCC:CCCCCCCCCC	(self)
6176605454	NC_000011.10:4914544:CCCCCCCC:CCCC… NC_000011.10:4914544:CCCCCCCC:CCCCCCCCCC	NC_000011.10:4914544:CCCCCCCC:CCCC… NC_000011.10:4914544:CCCCCCCC:CCCCCCCCCC	(self)
ss3691121932	NC_000011.10:4914545::CC	NC_000011.10:4914544:CCCCCCCC:CCCC… NC_000011.10:4914544:CCCCCCCC:CCCCCCCCCC	(self)

Removed from this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Destination RSIDs
ss3135900254	NC_000011.10:4914544:CC:	NC_000011.10:4914544:CCCCCCCC:CCCC… NC_000011.10:4914544:CCCCCCCC:CCCCCC

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

No publications for rs11318208

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.

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dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs11318208