Name: rs11266928
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.

rs11266928

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr7:97015048-97015058 (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: delCCC / delCC / delC / dupC / dup…
delCCC / delCC / delC / dupC / dupCC / dupCCC
Variation Type: Indel Insertion and Deletion
Frequency: delCC=0.2021 (1189/5882, ALFA)
delCC=0.4056 (1563/3854, ALSPAC)
(C)₁₁=0.4895 (1495/3054, 1000G)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: DLX6-AS1 : 2KB Upstream 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	5882	CCCCCCCCCCC=0.6078	CCCCCCCC=0.0000, CCCCCCCCC=0.2021, CCCCCCCCCC=0.1562, CCCCCCCCCCCC=0.0337, CCCCCCCCCCCCC=0.0002, CCCCCCCCCCCCCC=0.0000	0.629517	0.083969	0.286514	34
European	Sub	5682	CCCCCCCCCCC=0.5947	CCCCCCCC=0.0000, CCCCCCCCC=0.2091, CCCCCCCCCC=0.1614, CCCCCCCCCCCC=0.0347, CCCCCCCCCCCCC=0.0002, CCCCCCCCCCCCCC=0.0000	0.610814	0.08833	0.300857	29
African	Sub	90	CCCCCCCCCCC=1.00	CCCCCCCC=0.00, CCCCCCCCC=0.00, CCCCCCCCCC=0.00, CCCCCCCCCCCC=0.00, CCCCCCCCCCCCC=0.00, CCCCCCCCCCCCCC=0.00	1.0	0.0	0.0	N/A
African Others	Sub	2	CCCCCCCCCCC=1.0	CCCCCCCC=0.0, CCCCCCCCC=0.0, CCCCCCCCCC=0.0, CCCCCCCCCCCC=0.0, CCCCCCCCCCCCC=0.0, CCCCCCCCCCCCCC=0.0	1.0	0.0	0.0	N/A
African American	Sub	88	CCCCCCCCCCC=1.00	CCCCCCCC=0.00, CCCCCCCCC=0.00, CCCCCCCCCC=0.00, CCCCCCCCCCCC=0.00, CCCCCCCCCCCCC=0.00, CCCCCCCCCCCCCC=0.00	1.0	0.0	0.0	N/A
Asian	Sub	16	CCCCCCCCCCC=1.00	CCCCCCCC=0.00, CCCCCCCCC=0.00, CCCCCCCCCC=0.00, CCCCCCCCCCCC=0.00, CCCCCCCCCCCCC=0.00, CCCCCCCCCCCCCC=0.00	1.0	0.0	0.0	N/A
East Asian	Sub	10	CCCCCCCCCCC=1.0	CCCCCCCC=0.0, CCCCCCCCC=0.0, CCCCCCCCCC=0.0, CCCCCCCCCCCC=0.0, CCCCCCCCCCCCC=0.0, CCCCCCCCCCCCCC=0.0	1.0	0.0	0.0	N/A
Other Asian	Sub	6	CCCCCCCCCCC=1.0	CCCCCCCC=0.0, CCCCCCCCC=0.0, CCCCCCCCCC=0.0, CCCCCCCCCCCC=0.0, CCCCCCCCCCCCC=0.0, CCCCCCCCCCCCCC=0.0	1.0	0.0	0.0	N/A
Latin American 1	Sub	6	CCCCCCCCCCC=1.0	CCCCCCCC=0.0, CCCCCCCCC=0.0, CCCCCCCCCC=0.0, CCCCCCCCCCCC=0.0, CCCCCCCCCCCCC=0.0, CCCCCCCCCCCCCC=0.0	1.0	0.0	0.0	N/A
Latin American 2	Sub	32	CCCCCCCCCCC=1.00	CCCCCCCC=0.00, CCCCCCCCC=0.00, CCCCCCCCCC=0.00, CCCCCCCCCCCC=0.00, CCCCCCCCCCCCC=0.00, CCCCCCCCCCCCCC=0.00	1.0	0.0	0.0	N/A
South Asian	Sub	14	CCCCCCCCCCC=1.00	CCCCCCCC=0.00, CCCCCCCCC=0.00, CCCCCCCCCC=0.00, CCCCCCCCCCCC=0.00, CCCCCCCCCCCCC=0.00, CCCCCCCCCCCCCC=0.00	1.0	0.0	0.0	N/A
Other	Sub	42	CCCCCCCCCCC=0.90	CCCCCCCC=0.00, CCCCCCCCC=0.02, CCCCCCCCCC=0.05, CCCCCCCCCCCC=0.02, CCCCCCCCCCCCC=0.00, CCCCCCCCCCCCCC=0.00	0.944444	0.0	0.055556	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	5882	(C)₁₁=0.6078	delCCC=0.0000, delCC=0.2021, delC=0.1562, dupC=0.0337, dupCC=0.0002, dupCCC=0.0000
Allele Frequency Aggregator	European	Sub	5682	(C)₁₁=0.5947	delCCC=0.0000, delCC=0.2091, delC=0.1614, dupC=0.0347, dupCC=0.0002, dupCCC=0.0000
Allele Frequency Aggregator	African	Sub	90	(C)₁₁=1.00	delCCC=0.00, delCC=0.00, delC=0.00, dupC=0.00, dupCC=0.00, dupCCC=0.00
Allele Frequency Aggregator	Other	Sub	42	(C)₁₁=0.90	delCCC=0.00, delCC=0.02, delC=0.05, dupC=0.02, dupCC=0.00, dupCCC=0.00
Allele Frequency Aggregator	Latin American 2	Sub	32	(C)₁₁=1.00	delCCC=0.00, delCC=0.00, delC=0.00, dupC=0.00, dupCC=0.00, dupCCC=0.00
Allele Frequency Aggregator	Asian	Sub	16	(C)₁₁=1.00	delCCC=0.00, delCC=0.00, delC=0.00, dupC=0.00, dupCC=0.00, dupCCC=0.00
Allele Frequency Aggregator	South Asian	Sub	14	(C)₁₁=1.00	delCCC=0.00, delCC=0.00, delC=0.00, dupC=0.00, dupCC=0.00, dupCCC=0.00
Allele Frequency Aggregator	Latin American 1	Sub	6	(C)₁₁=1.0	delCCC=0.0, delCC=0.0, delC=0.0, dupC=0.0, dupCC=0.0, dupCCC=0.0
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	(C)₁₁=0.5944	delCC=0.4056
1000Genomes	Global	Study-wide	3054	(C)₁₁=0.4895	delCC=0.5105
1000Genomes	Europe	Sub	738	(C)₁₁=0.575	delCC=0.425
1000Genomes	African	Sub	707	(C)₁₁=0.325	delCC=0.675
1000Genomes	South Asian	Sub	593	(C)₁₁=0.659	delCC=0.341
1000Genomes	East Asian	Sub	557	(C)₁₁=0.549	delCC=0.451
1000Genomes	American	Sub	459	(C)₁₁=0.314	delCC=0.686

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 7	NC_000007.14:g.97015056_97015058del
GRCh38.p14 chr 7	NC_000007.14:g.97015057_97015058del
GRCh38.p14 chr 7	NC_000007.14:g.97015058del
GRCh38.p14 chr 7	NC_000007.14:g.97015058dup
GRCh38.p14 chr 7	NC_000007.14:g.97015057_97015058dup
GRCh38.p14 chr 7	NC_000007.14:g.97015056_97015058dup
GRCh37.p13 chr 7	NC_000007.13:g.96644368_96644370del
GRCh37.p13 chr 7	NC_000007.13:g.96644369_96644370del
GRCh37.p13 chr 7	NC_000007.13:g.96644370del
GRCh37.p13 chr 7	NC_000007.13:g.96644370dup
GRCh37.p13 chr 7	NC_000007.13:g.96644369_96644370dup
GRCh37.p13 chr 7	NC_000007.13:g.96644368_96644370dup

Gene: DLX6-AS1, DLX6 antisense RNA 1 (minus strand) : 2KB Upstream Variant

Molecule type	Change	Amino acid[Codon]	SO Term
DLX6-AS1 transcript	NR_015448.1:n.	N/A	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	(C)₁₁=	delCCC	delCC	delC	dupC	dupCC	dupCCC
GRCh38.p14 chr 7	NC_000007.14:g.97015048_97015058=	NC_000007.14:g.97015056_97015058del	NC_000007.14:g.97015057_97015058del	NC_000007.14:g.97015058del	NC_000007.14:g.97015058dup	NC_000007.14:g.97015057_97015058dup	NC_000007.14:g.97015056_97015058dup
GRCh37.p13 chr 7	NC_000007.13:g.96644360_96644370=	NC_000007.13:g.96644368_96644370del	NC_000007.13:g.96644369_96644370del	NC_000007.13:g.96644370del	NC_000007.13:g.96644370dup	NC_000007.13:g.96644369_96644370dup	NC_000007.13:g.96644368_96644370dup

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#.

68 SubSNP, 25 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	ABI	ss43111992	Mar 15, 2016 (147)
2	HGSV	ss77973954	Aug 21, 2014 (142)
3	HGSV	ss81041573	Aug 21, 2014 (142)
4	HGSV	ss83111063	Dec 15, 2007 (130)
5	HGSV	ss83814311	Dec 15, 2007 (130)
6	HUMANGENOME_JCVI	ss95468987	Feb 05, 2009 (130)
7	HUMANGENOME_JCVI	ss98211577	Mar 15, 2016 (147)
8	BUSHMAN	ss193934867	Jul 04, 2010 (132)
9	GMI	ss287817138	Mar 15, 2016 (147)
10	GMI	ss288859884	May 04, 2012 (138)
11	GMI	ss288859885	May 04, 2012 (137)
12	PJP	ss295347575	May 09, 2011 (134)
13	1000GENOMES	ss1377403508	Aug 21, 2014 (142)
14	1000GENOMES	ss1377403511	Aug 21, 2014 (142)
15	DDI	ss1536556524	Apr 01, 2015 (144)
16	EVA_UK10K_ALSPAC	ss1705741660	Apr 01, 2015 (144)
17	EVA_UK10K_TWINSUK	ss1705741880	Apr 01, 2015 (144)
18	EVA_UK10K_ALSPAC	ss1710338496	Apr 01, 2015 (144)
19	EVA_UK10K_TWINSUK	ss1710342544	Apr 01, 2015 (144)
20	HAMMER_LAB	ss1805125297	Sep 08, 2015 (146)
21	HAMMER_LAB	ss1805125298	Sep 08, 2015 (146)
22	SWEGEN	ss3001675122	Nov 08, 2017 (151)
23	MCHAISSO	ss3064266086	Nov 08, 2017 (151)
24	MCHAISSO	ss3065148973	Nov 08, 2017 (151)
25	MCHAISSO	ss3065148974	Nov 08, 2017 (151)
26	MCHAISSO	ss3066158633	Nov 08, 2017 (151)
27	BEROUKHIMLAB	ss3644244269	Oct 12, 2018 (152)
28	BIOINF_KMB_FNS_UNIBA	ss3646045447	Oct 12, 2018 (152)
29	EVA_DECODE	ss3720261918	Jul 13, 2019 (153)
30	EVA_DECODE	ss3720261919	Jul 13, 2019 (153)
31	EVA_DECODE	ss3720261920	Jul 13, 2019 (153)
32	PACBIO	ss3785900143	Jul 13, 2019 (153)
33	PACBIO	ss3791189455	Jul 13, 2019 (153)
34	PACBIO	ss3796069447	Jul 13, 2019 (153)
35	KHV_HUMAN_GENOMES	ss3810074825	Jul 13, 2019 (153)
36	KHV_HUMAN_GENOMES	ss3810074826	Jul 13, 2019 (153)
37	KHV_HUMAN_GENOMES	ss3810074827	Jul 13, 2019 (153)
38	KOGIC	ss3962146017	Apr 26, 2020 (154)
39	KOGIC	ss3962146018	Apr 26, 2020 (154)
40	KOGIC	ss3962146019	Apr 26, 2020 (154)
41	KOGIC	ss3962146020	Apr 26, 2020 (154)
42	GNOMAD	ss4169033916	Apr 26, 2021 (155)
43	GNOMAD	ss4169033917	Apr 26, 2021 (155)
44	GNOMAD	ss4169033918	Apr 26, 2021 (155)
45	GNOMAD	ss4169033919	Apr 26, 2021 (155)
46	GNOMAD	ss4169033920	Apr 26, 2021 (155)
47	GNOMAD	ss4169033921	Apr 26, 2021 (155)
48	TOMMO_GENOMICS	ss5184570467	Apr 26, 2021 (155)
49	TOMMO_GENOMICS	ss5184570468	Apr 26, 2021 (155)
50	TOMMO_GENOMICS	ss5184570469	Apr 26, 2021 (155)
51	TOMMO_GENOMICS	ss5184570470	Apr 26, 2021 (155)
52	TOMMO_GENOMICS	ss5184570471	Apr 26, 2021 (155)
53	1000G_HIGH_COVERAGE	ss5273962166	Oct 13, 2022 (156)
54	1000G_HIGH_COVERAGE	ss5273962167	Oct 13, 2022 (156)
55	1000G_HIGH_COVERAGE	ss5273962168	Oct 13, 2022 (156)
56	1000G_HIGH_COVERAGE	ss5273962169	Oct 13, 2022 (156)
57	1000G_HIGH_COVERAGE	ss5273962170	Oct 13, 2022 (156)
58	HUGCELL_USP	ss5470941965	Oct 13, 2022 (156)
59	HUGCELL_USP	ss5470941966	Oct 13, 2022 (156)
60	HUGCELL_USP	ss5470941967	Oct 13, 2022 (156)
61	TOMMO_GENOMICS	ss5725250735	Oct 13, 2022 (156)
62	TOMMO_GENOMICS	ss5725250736	Oct 13, 2022 (156)
63	TOMMO_GENOMICS	ss5725250737	Oct 13, 2022 (156)
64	TOMMO_GENOMICS	ss5725250738	Oct 13, 2022 (156)
65	TOMMO_GENOMICS	ss5725250739	Oct 13, 2022 (156)
66	EVA	ss5823229106	Oct 13, 2022 (156)
67	EVA	ss5823229107	Oct 13, 2022 (156)
68	EVA	ss5860011875	Oct 13, 2022 (156)
69	1000Genomes	NC_000007.13 - 96644360	Oct 12, 2018 (152)
70	The Avon Longitudinal Study of Parents and Children	NC_000007.13 - 96644360	Oct 12, 2018 (152)
71	gnomAD - Genomes Submission ignored due to conflicting rows: Row 270078182 (NC_000007.14:97015047::C 4299/134396) Row 270078183 (NC_000007.14:97015047::CC 91/134674) Row 270078184 (NC_000007.14:97015047::CCC 1/134684)...	-	Apr 26, 2021 (155)
72	gnomAD - Genomes Submission ignored due to conflicting rows: Row 270078182 (NC_000007.14:97015047::C 4299/134396) Row 270078183 (NC_000007.14:97015047::CC 91/134674) Row 270078184 (NC_000007.14:97015047::CCC 1/134684)...	-	Apr 26, 2021 (155)
73	gnomAD - Genomes Submission ignored due to conflicting rows: Row 270078182 (NC_000007.14:97015047::C 4299/134396) Row 270078183 (NC_000007.14:97015047::CC 91/134674) Row 270078184 (NC_000007.14:97015047::CCC 1/134684)...	-	Apr 26, 2021 (155)
74	gnomAD - Genomes Submission ignored due to conflicting rows: Row 270078182 (NC_000007.14:97015047::C 4299/134396) Row 270078183 (NC_000007.14:97015047::CC 91/134674) Row 270078184 (NC_000007.14:97015047::CCC 1/134684)...	-	Apr 26, 2021 (155)
75	gnomAD - Genomes Submission ignored due to conflicting rows: Row 270078182 (NC_000007.14:97015047::C 4299/134396) Row 270078183 (NC_000007.14:97015047::CC 91/134674) Row 270078184 (NC_000007.14:97015047::CCC 1/134684)...	-	Apr 26, 2021 (155)
76	gnomAD - Genomes Submission ignored due to conflicting rows: Row 270078182 (NC_000007.14:97015047::C 4299/134396) Row 270078183 (NC_000007.14:97015047::CC 91/134674) Row 270078184 (NC_000007.14:97015047::CCC 1/134684)...	-	Apr 26, 2021 (155)
77	Korean Genome Project Submission ignored due to conflicting rows: Row 18524018 (NC_000007.14:97015048:C: 796/1832) Row 18524019 (NC_000007.14:97015049::CC 4/1832) Row 18524020 (NC_000007.14:97015047:CC: 577/1832)...	-	Apr 26, 2020 (154)
78	Korean Genome Project Submission ignored due to conflicting rows: Row 18524018 (NC_000007.14:97015048:C: 796/1832) Row 18524019 (NC_000007.14:97015049::CC 4/1832) Row 18524020 (NC_000007.14:97015047:CC: 577/1832)...	-	Apr 26, 2020 (154)
79	Korean Genome Project Submission ignored due to conflicting rows: Row 18524018 (NC_000007.14:97015048:C: 796/1832) Row 18524019 (NC_000007.14:97015049::CC 4/1832) Row 18524020 (NC_000007.14:97015047:CC: 577/1832)...	-	Apr 26, 2020 (154)
80	Korean Genome Project Submission ignored due to conflicting rows: Row 18524018 (NC_000007.14:97015048:C: 796/1832) Row 18524019 (NC_000007.14:97015049::CC 4/1832) Row 18524020 (NC_000007.14:97015047:CC: 577/1832)...	-	Apr 26, 2020 (154)
81	8.3KJPN Submission ignored due to conflicting rows: Row 42539774 (NC_000007.13:96644359:CC: 5617/16754) Row 42539775 (NC_000007.13:96644359:C: 6509/16754) Row 42539776 (NC_000007.13:96644359::CC 25/16754)...	-	Apr 26, 2021 (155)
82	8.3KJPN Submission ignored due to conflicting rows: Row 42539774 (NC_000007.13:96644359:CC: 5617/16754) Row 42539775 (NC_000007.13:96644359:C: 6509/16754) Row 42539776 (NC_000007.13:96644359::CC 25/16754)...	-	Apr 26, 2021 (155)
83	8.3KJPN Submission ignored due to conflicting rows: Row 42539774 (NC_000007.13:96644359:CC: 5617/16754) Row 42539775 (NC_000007.13:96644359:C: 6509/16754) Row 42539776 (NC_000007.13:96644359::CC 25/16754)...	-	Apr 26, 2021 (155)
84	8.3KJPN Submission ignored due to conflicting rows: Row 42539774 (NC_000007.13:96644359:CC: 5617/16754) Row 42539775 (NC_000007.13:96644359:C: 6509/16754) Row 42539776 (NC_000007.13:96644359::CC 25/16754)...	-	Apr 26, 2021 (155)
85	8.3KJPN Submission ignored due to conflicting rows: Row 42539774 (NC_000007.13:96644359:CC: 5617/16754) Row 42539775 (NC_000007.13:96644359:C: 6509/16754) Row 42539776 (NC_000007.13:96644359::CC 25/16754)...	-	Apr 26, 2021 (155)
86	14KJPN Submission ignored due to conflicting rows: Row 59087839 (NC_000007.14:97015047:CC: 9437/28254) Row 59087840 (NC_000007.14:97015047:C: 10964/28254) Row 59087841 (NC_000007.14:97015047::C 227/28254)...	-	Oct 13, 2022 (156)
87	14KJPN Submission ignored due to conflicting rows: Row 59087839 (NC_000007.14:97015047:CC: 9437/28254) Row 59087840 (NC_000007.14:97015047:C: 10964/28254) Row 59087841 (NC_000007.14:97015047::C 227/28254)...	-	Oct 13, 2022 (156)
88	14KJPN Submission ignored due to conflicting rows: Row 59087839 (NC_000007.14:97015047:CC: 9437/28254) Row 59087840 (NC_000007.14:97015047:C: 10964/28254) Row 59087841 (NC_000007.14:97015047::C 227/28254)...	-	Oct 13, 2022 (156)
89	14KJPN Submission ignored due to conflicting rows: Row 59087839 (NC_000007.14:97015047:CC: 9437/28254) Row 59087840 (NC_000007.14:97015047:C: 10964/28254) Row 59087841 (NC_000007.14:97015047::C 227/28254)...	-	Oct 13, 2022 (156)
90	14KJPN Submission ignored due to conflicting rows: Row 59087839 (NC_000007.14:97015047:CC: 9437/28254) Row 59087840 (NC_000007.14:97015047:C: 10964/28254) Row 59087841 (NC_000007.14:97015047::C 227/28254)...	-	Oct 13, 2022 (156)
91	UK 10K study - Twins	-	Oct 12, 2018 (152)
92	UK 10K study - Twins Submission ignored due to conflicting rows: Row 21299154 (NC_000007.13:96644359:CC: 1451/3708) Row 21299155 (NC_000007.13:96644360:C: 1015/3708)	-	Apr 26, 2020 (154)
93	ALFA	NC_000007.14 - 97015048	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)
rs55633866	Dec 02, 2009 (131)
rs58870153	May 25, 2008 (130)
rs59460054	May 25, 2008 (130)
rs72017224	Oct 11, 2011 (135)
rs200157353	May 13, 2013 (138)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss5184570471	NC_000007.13:96644359:CCC:	NC_000007.14:97015047:CCCCCCCCCCC:… NC_000007.14:97015047:CCCCCCCCCCC:CCCCCCCC	(self)
ss4169033921, ss5273962169, ss5725250739	NC_000007.14:97015047:CCC:	NC_000007.14:97015047:CCCCCCCCCCC:… NC_000007.14:97015047:CCCCCCCCCCC:CCCCCCCC	(self)
205311416	NC_000007.14:97015047:CCCCCCCCCCC:… NC_000007.14:97015047:CCCCCCCCCCC:CCCCCCCC	NC_000007.14:97015047:CCCCCCCCCCC:… NC_000007.14:97015047:CCCCCCCCCCC:CCCCCCCC	(self)
ss83111063, ss83814311	NC_000007.11:96289019:CC:	NC_000007.14:97015047:CCCCCCCCCCC:… NC_000007.14:97015047:CCCCCCCCCCC:CCCCCCCCC	(self)
ss288859885	NC_000007.12:96482295:CC:	NC_000007.14:97015047:CCCCCCCCCCC:… NC_000007.14:97015047:CCCCCCCCCCC:CCCCCCCCC	(self)
38274104, 21299154, ss1377403508, ss1536556524, ss1705741660, ss1705741880, ss1805125298, ss3001675122, ss3644244269, ss3785900143, ss3791189455, ss3796069447, ss5184570467, ss5823229106	NC_000007.13:96644359:CC:	NC_000007.14:97015047:CCCCCCCCCCC:… NC_000007.14:97015047:CCCCCCCCCCC:CCCCCCCCC	(self)
ss3064266086, ss3065148973, ss3065148974, ss3066158633, ss3646045447, ss3720261920, ss3810074826, ss3962146019, ss4169033920, ss5273962166, ss5470941967, ss5725250735, ss5860011875	NC_000007.14:97015047:CC:	NC_000007.14:97015047:CCCCCCCCCCC:… NC_000007.14:97015047:CCCCCCCCCCC:CCCCCCCCC	(self)
205311416	NC_000007.14:97015047:CCCCCCCCCCC:… NC_000007.14:97015047:CCCCCCCCCCC:CCCCCCCCC	NC_000007.14:97015047:CCCCCCCCCCC:… NC_000007.14:97015047:CCCCCCCCCCC:CCCCCCCCC	(self)
ss287817138	NT_007933.15:34677202:CC:	NC_000007.14:97015047:CCCCCCCCCCC:… NC_000007.14:97015047:CCCCCCCCCCC:CCCCCCCCC	(self)
ss43111992, ss95468987, ss98211577	NT_007933.15:34677211:CC:	NC_000007.14:97015047:CCCCCCCCCCC:… NC_000007.14:97015047:CCCCCCCCCCC:CCCCCCCCC	(self)
ss77973954, ss81041573	NC_000007.11:96289020:C:	NC_000007.14:97015047:CCCCCCCCCCC:… NC_000007.14:97015047:CCCCCCCCCCC:CCCCCCCCCC	(self)
ss288859884, ss295347575	NC_000007.12:96482295:C:	NC_000007.14:97015047:CCCCCCCCCCC:… NC_000007.14:97015047:CCCCCCCCCCC:CCCCCCCCCC	(self)
ss1805125297, ss5184570468, ss5823229107	NC_000007.13:96644359:C:	NC_000007.14:97015047:CCCCCCCCCCC:… NC_000007.14:97015047:CCCCCCCCCCC:CCCCCCCCCC	(self)
ss1377403511, ss1710338496, ss1710342544	NC_000007.13:96644360:C:	NC_000007.14:97015047:CCCCCCCCCCC:… NC_000007.14:97015047:CCCCCCCCCCC:CCCCCCCCCC	(self)
ss4169033919, ss5273962167, ss5470941966, ss5725250736	NC_000007.14:97015047:C:	NC_000007.14:97015047:CCCCCCCCCCC:… NC_000007.14:97015047:CCCCCCCCCCC:CCCCCCCCCC	(self)
205311416	NC_000007.14:97015047:CCCCCCCCCCC:… NC_000007.14:97015047:CCCCCCCCCCC:CCCCCCCCCC	NC_000007.14:97015047:CCCCCCCCCCC:… NC_000007.14:97015047:CCCCCCCCCCC:CCCCCCCCCC	(self)
ss3720261919, ss3810074825, ss3962146017	NC_000007.14:97015048:C:	NC_000007.14:97015047:CCCCCCCCCCC:… NC_000007.14:97015047:CCCCCCCCCCC:CCCCCCCCCC	(self)
ss43111992, ss98211577	NT_007933.15:34677211:CC:C	NC_000007.14:97015047:CCCCCCCCCCC:… NC_000007.14:97015047:CCCCCCCCCCC:CCCCCCCCCC	(self)
ss193934867	NT_007933.16:34508268:C:	NC_000007.14:97015047:CCCCCCCCCCC:… NC_000007.14:97015047:CCCCCCCCCCC:CCCCCCCCCC	(self)
ss5184570470	NC_000007.13:96644359::C	NC_000007.14:97015047:CCCCCCCCCCC:… NC_000007.14:97015047:CCCCCCCCCCC:CCCCCCCCCCCC	(self)
ss4169033916, ss5273962168, ss5470941965, ss5725250737	NC_000007.14:97015047::C	NC_000007.14:97015047:CCCCCCCCCCC:… NC_000007.14:97015047:CCCCCCCCCCC:CCCCCCCCCCCC	(self)
205311416	NC_000007.14:97015047:CCCCCCCCCCC:… NC_000007.14:97015047:CCCCCCCCCCC:CCCCCCCCCCCC	NC_000007.14:97015047:CCCCCCCCCCC:… NC_000007.14:97015047:CCCCCCCCCCC:CCCCCCCCCCCC	(self)
ss3720261918, ss3810074827, ss3962146020	NC_000007.14:97015049::C	NC_000007.14:97015047:CCCCCCCCCCC:… NC_000007.14:97015047:CCCCCCCCCCC:CCCCCCCCCCCC	(self)
ss5184570469	NC_000007.13:96644359::CC	NC_000007.14:97015047:CCCCCCCCCCC:… NC_000007.14:97015047:CCCCCCCCCCC:CCCCCCCCCCCCC	(self)
ss4169033917, ss5273962170, ss5725250738	NC_000007.14:97015047::CC	NC_000007.14:97015047:CCCCCCCCCCC:… NC_000007.14:97015047:CCCCCCCCCCC:CCCCCCCCCCCCC	(self)
205311416	NC_000007.14:97015047:CCCCCCCCCCC:… NC_000007.14:97015047:CCCCCCCCCCC:CCCCCCCCCCCCC	NC_000007.14:97015047:CCCCCCCCCCC:… NC_000007.14:97015047:CCCCCCCCCCC:CCCCCCCCCCCCC	(self)
ss3962146018	NC_000007.14:97015049::CC	NC_000007.14:97015047:CCCCCCCCCCC:… NC_000007.14:97015047:CCCCCCCCCCC:CCCCCCCCCCCCC	(self)
ss4169033918	NC_000007.14:97015047::CCC	NC_000007.14:97015047:CCCCCCCCCCC:… NC_000007.14:97015047:CCCCCCCCCCC:CCCCCCCCCCCCCC	(self)
205311416	NC_000007.14:97015047:CCCCCCCCCCC:… NC_000007.14:97015047:CCCCCCCCCCC:CCCCCCCCCCCCCC	NC_000007.14:97015047:CCCCCCCCCCC:… NC_000007.14:97015047:CCCCCCCCCCC:CCCCCCCCCCCCCC	(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 rs11266928

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

rs11266928