Name: rs11308911
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.

rs11308911

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr4:15381422-15381436 (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: delAA / delA / dupA / dupAA / dupA…
delAA / delA / dupA / dupAA / dupAAA / dup(A)₄ / dup(A)₅ / dup(A)₁₁
Variation Type: Indel Insertion and Deletion
Frequency: delAA=0.0000 (0/3898, ALFA)
delA=0.0000 (0/3898, ALFA)
dupA=0.0000 (0/3898, ALFA) (+ 3 more)
dupAA=0.0000 (0/3898, ALFA)
dupAAA=0.0000 (0/3898, ALFA)
dup(A)₄=0.0000 (0/3898, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: C1QTNF7 : Intron Variant
C1QTNF7-AS1 : 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	3898	AAAAAAAAAAAAAAA=1.0000	AAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAA=0.0000	1.0	N/A
European	Sub	3246	AAAAAAAAAAAAAAA=1.0000	AAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAA=0.0000	1.0	N/A
African	Sub	292	AAAAAAAAAAAAAAA=1.000	AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000	1.0	N/A
African Others	Sub	12	AAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
African American	Sub	280	AAAAAAAAAAAAAAA=1.000	AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000	1.0	N/A
Asian	Sub	22	AAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
East Asian	Sub	20	AAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Other Asian	Sub	2	AAAAAAAAAAAAAAA=1.0	AAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAA=0.0	1.0	N/A
Latin American 1	Sub	58	AAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Latin American 2	Sub	110	AAAAAAAAAAAAAAA=1.000	AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000	1.0	N/A
South Asian	Sub	20	AAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Other	Sub	150	AAAAAAAAAAAAAAA=1.000	AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000	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
Allele Frequency Aggregator	Total	Global	3898	(A)₁₅=1.0000	delAA=0.0000, delA=0.0000, dupA=0.0000, dupAA=0.0000, dupAAA=0.0000, dup(A)₄=0.0000
Allele Frequency Aggregator	European	Sub	3246	(A)₁₅=1.0000	delAA=0.0000, delA=0.0000, dupA=0.0000, dupAA=0.0000, dupAAA=0.0000, dup(A)₄=0.0000
Allele Frequency Aggregator	African	Sub	292	(A)₁₅=1.000	delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000, dupAAA=0.000, dup(A)₄=0.000
Allele Frequency Aggregator	Other	Sub	150	(A)₁₅=1.000	delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000, dupAAA=0.000, dup(A)₄=0.000
Allele Frequency Aggregator	Latin American 2	Sub	110	(A)₁₅=1.000	delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000, dupAAA=0.000, dup(A)₄=0.000
Allele Frequency Aggregator	Latin American 1	Sub	58	(A)₁₅=1.00	delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00, dup(A)₄=0.00
Allele Frequency Aggregator	Asian	Sub	22	(A)₁₅=1.00	delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00, dup(A)₄=0.00
Allele Frequency Aggregator	South Asian	Sub	20	(A)₁₅=1.00	delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00, dup(A)₄=0.00

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 4	NC_000004.12:g.15381435_15381436del
GRCh38.p14 chr 4	NC_000004.12:g.15381436del
GRCh38.p14 chr 4	NC_000004.12:g.15381436dup
GRCh38.p14 chr 4	NC_000004.12:g.15381435_15381436dup
GRCh38.p14 chr 4	NC_000004.12:g.15381434_15381436dup
GRCh38.p14 chr 4	NC_000004.12:g.15381433_15381436dup
GRCh38.p14 chr 4	NC_000004.12:g.15381432_15381436dup
GRCh38.p14 chr 4	NC_000004.12:g.15381426_15381436dup
GRCh37.p13 chr 4	NC_000004.11:g.15383059_15383060del
GRCh37.p13 chr 4	NC_000004.11:g.15383060del
GRCh37.p13 chr 4	NC_000004.11:g.15383060dup
GRCh37.p13 chr 4	NC_000004.11:g.15383059_15383060dup
GRCh37.p13 chr 4	NC_000004.11:g.15383058_15383060dup
GRCh37.p13 chr 4	NC_000004.11:g.15383057_15383060dup
GRCh37.p13 chr 4	NC_000004.11:g.15383056_15383060dup
GRCh37.p13 chr 4	NC_000004.11:g.15383050_15383060dup

Gene: C1QTNF7, C1q and TNF related 7 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
C1QTNF7 transcript variant 1	NM_001135170.2:c.13+41228… NM_001135170.2:c.13+41228_13+41229del	N/A	Intron Variant
C1QTNF7 transcript variant 2	NM_001135171.2:c.-9+6666_… NM_001135171.2:c.-9+6666_-9+6667del	N/A	Intron Variant
C1QTNF7 transcript variant 3	NM_031911.5:c.	N/A	Genic Upstream Transcript Variant
C1QTNF7 transcript variant X1	XM_011513772.2:c.13+41228… XM_011513772.2:c.13+41228_13+41229del	N/A	Intron Variant
C1QTNF7 transcript variant X2	XM_047449566.1:c.-9+6666_… XM_047449566.1:c.-9+6666_-9+6667del	N/A	Intron Variant
C1QTNF7 transcript variant X3	XM_011513773.2:c.	N/A	Genic Upstream Transcript Variant

Gene: C1QTNF7-AS1, C1QTNF7 antisense RNA 1 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
C1QTNF7-AS1 transcript	NR_125911.1: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)₁₅=	delAA	delA	dupA	dupAA	dupAAA	dup(A)₄	dup(A)₅	dup(A)₁₁
GRCh38.p14 chr 4	NC_000004.12:g.15381422_15381436=	NC_000004.12:g.15381435_15381436del	NC_000004.12:g.15381436del	NC_000004.12:g.15381436dup	NC_000004.12:g.15381435_15381436dup	NC_000004.12:g.15381434_15381436dup	NC_000004.12:g.15381433_15381436dup	NC_000004.12:g.15381432_15381436dup	NC_000004.12:g.15381426_15381436dup
GRCh37.p13 chr 4	NC_000004.11:g.15383046_15383060=	NC_000004.11:g.15383059_15383060del	NC_000004.11:g.15383060del	NC_000004.11:g.15383060dup	NC_000004.11:g.15383059_15383060dup	NC_000004.11:g.15383058_15383060dup	NC_000004.11:g.15383057_15383060dup	NC_000004.11:g.15383056_15383060dup	NC_000004.11:g.15383050_15383060dup
C1QTNF7 transcript variant 1	NM_001135170.1:c.13+41215=	NM_001135170.1:c.13+41228_13+41229del	NM_001135170.1:c.13+41229del	NM_001135170.1:c.13+41229dup	NM_001135170.1:c.13+41228_13+41229dup	NM_001135170.1:c.13+41227_13+41229dup	NM_001135170.1:c.13+41226_13+41229dup	NM_001135170.1:c.13+41225_13+41229dup	NM_001135170.1:c.13+41219_13+41229dup
C1QTNF7 transcript variant 1	NM_001135170.2:c.13+41215=	NM_001135170.2:c.13+41228_13+41229del	NM_001135170.2:c.13+41229del	NM_001135170.2:c.13+41229dup	NM_001135170.2:c.13+41228_13+41229dup	NM_001135170.2:c.13+41227_13+41229dup	NM_001135170.2:c.13+41226_13+41229dup	NM_001135170.2:c.13+41225_13+41229dup	NM_001135170.2:c.13+41219_13+41229dup
C1QTNF7 transcript variant 2	NM_001135171.1:c.-9+6653=	NM_001135171.1:c.-9+6666_-9+6667del	NM_001135171.1:c.-9+6667del	NM_001135171.1:c.-9+6667dup	NM_001135171.1:c.-9+6666_-9+6667dup	NM_001135171.1:c.-9+6665_-9+6667dup	NM_001135171.1:c.-9+6664_-9+6667dup	NM_001135171.1:c.-9+6663_-9+6667dup	NM_001135171.1:c.-9+6657_-9+6667dup
C1QTNF7 transcript variant 2	NM_001135171.2:c.-9+6653=	NM_001135171.2:c.-9+6666_-9+6667del	NM_001135171.2:c.-9+6667del	NM_001135171.2:c.-9+6667dup	NM_001135171.2:c.-9+6666_-9+6667dup	NM_001135171.2:c.-9+6665_-9+6667dup	NM_001135171.2:c.-9+6664_-9+6667dup	NM_001135171.2:c.-9+6663_-9+6667dup	NM_001135171.2:c.-9+6657_-9+6667dup
C1QTNF7 transcript variant X1	XM_011513772.2:c.13+41215=	XM_011513772.2:c.13+41228_13+41229del	XM_011513772.2:c.13+41229del	XM_011513772.2:c.13+41229dup	XM_011513772.2:c.13+41228_13+41229dup	XM_011513772.2:c.13+41227_13+41229dup	XM_011513772.2:c.13+41226_13+41229dup	XM_011513772.2:c.13+41225_13+41229dup	XM_011513772.2:c.13+41219_13+41229dup
C1QTNF7 transcript variant X2	XM_047449566.1:c.-9+6653=	XM_047449566.1:c.-9+6666_-9+6667del	XM_047449566.1:c.-9+6667del	XM_047449566.1:c.-9+6667dup	XM_047449566.1:c.-9+6666_-9+6667dup	XM_047449566.1:c.-9+6665_-9+6667dup	XM_047449566.1:c.-9+6664_-9+6667dup	XM_047449566.1:c.-9+6663_-9+6667dup	XM_047449566.1:c.-9+6657_-9+6667dup

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#.

66 SubSNP, 30 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	HGSV	ss82875088	Dec 14, 2007 (137)
2	HUMANGENOME_JCVI	ss95346914	Oct 12, 2018 (152)
3	GMI	ss288487418	Oct 12, 2018 (152)
4	PJP	ss295153659	May 31, 2013 (138)
5	PJP	ss295153660	May 31, 2013 (138)
6	SSMP	ss663470258	Apr 01, 2015 (144)
7	BILGI_BIOE	ss666246597	Apr 25, 2013 (138)
8	EVA_UK10K_ALSPAC	ss1704055387	Apr 01, 2015 (144)
9	EVA_UK10K_ALSPAC	ss1704055389	Apr 01, 2015 (144)
10	EVA_UK10K_TWINSUK	ss1704055468	Apr 01, 2015 (144)
11	EVA_UK10K_TWINSUK	ss1704055471	Apr 01, 2015 (144)
12	SYSTEMSBIOZJU	ss2625548807	Nov 08, 2017 (151)
13	SWEGEN	ss2994203460	Nov 08, 2017 (151)
14	SWEGEN	ss2994203461	Nov 08, 2017 (151)
15	SWEGEN	ss2994203462	Nov 08, 2017 (151)
16	MCHAISSO	ss3065934798	Nov 08, 2017 (151)
17	URBANLAB	ss3647661040	Oct 12, 2018 (152)
18	EVA_DECODE	ss3711481849	Jul 13, 2019 (153)
19	EVA_DECODE	ss3711481850	Jul 13, 2019 (153)
20	EVA_DECODE	ss3711481851	Jul 13, 2019 (153)
21	EVA_DECODE	ss3711481852	Jul 13, 2019 (153)
22	EVA_DECODE	ss3711481853	Jul 13, 2019 (153)
23	EVA_DECODE	ss3711481854	Jul 13, 2019 (153)
24	ACPOP	ss3730890067	Jul 13, 2019 (153)
25	ACPOP	ss3730890068	Jul 13, 2019 (153)
26	ACPOP	ss3730890069	Jul 13, 2019 (153)
27	PACBIO	ss3784630019	Jul 13, 2019 (153)
28	EVA	ss3828389898	Apr 26, 2020 (154)
29	EVA	ss3837628261	Apr 26, 2020 (154)
30	EVA	ss3843062435	Apr 26, 2020 (154)
31	KOGIC	ss3953602329	Apr 26, 2020 (154)
32	KOGIC	ss3953602330	Apr 26, 2020 (154)
33	KOGIC	ss3953602331	Apr 26, 2020 (154)
34	KOGIC	ss3953602332	Apr 26, 2020 (154)
35	KOGIC	ss3953602333	Apr 26, 2020 (154)
36	GNOMAD	ss4091208704	Apr 26, 2021 (155)
37	GNOMAD	ss4091208705	Apr 26, 2021 (155)
38	GNOMAD	ss4091208706	Apr 26, 2021 (155)
39	GNOMAD	ss4091208707	Apr 26, 2021 (155)
40	GNOMAD	ss4091208708	Apr 26, 2021 (155)
41	GNOMAD	ss4091208709	Apr 26, 2021 (155)
42	GNOMAD	ss4091208710	Apr 26, 2021 (155)
43	TOMMO_GENOMICS	ss5164373340	Apr 26, 2021 (155)
44	TOMMO_GENOMICS	ss5164373341	Apr 26, 2021 (155)
45	TOMMO_GENOMICS	ss5164373342	Apr 26, 2021 (155)
46	TOMMO_GENOMICS	ss5164373343	Apr 26, 2021 (155)
47	TOMMO_GENOMICS	ss5164373344	Apr 26, 2021 (155)
48	1000G_HIGH_COVERAGE	ss5258180562	Oct 13, 2022 (156)
49	1000G_HIGH_COVERAGE	ss5258180563	Oct 13, 2022 (156)
50	1000G_HIGH_COVERAGE	ss5258180564	Oct 13, 2022 (156)
51	1000G_HIGH_COVERAGE	ss5258180565	Oct 13, 2022 (156)
52	1000G_HIGH_COVERAGE	ss5258180566	Oct 13, 2022 (156)
53	1000G_HIGH_COVERAGE	ss5258180567	Oct 13, 2022 (156)
54	HUGCELL_USP	ss5457064567	Oct 13, 2022 (156)
55	HUGCELL_USP	ss5457064568	Oct 13, 2022 (156)
56	HUGCELL_USP	ss5457064569	Oct 13, 2022 (156)
57	HUGCELL_USP	ss5457064570	Oct 13, 2022 (156)
58	HUGCELL_USP	ss5457064571	Oct 13, 2022 (156)
59	TOMMO_GENOMICS	ss5698070535	Oct 13, 2022 (156)
60	TOMMO_GENOMICS	ss5698070536	Oct 13, 2022 (156)
61	TOMMO_GENOMICS	ss5698070537	Oct 13, 2022 (156)
62	TOMMO_GENOMICS	ss5698070538	Oct 13, 2022 (156)
63	TOMMO_GENOMICS	ss5698070539	Oct 13, 2022 (156)
64	EVA	ss5843605016	Oct 13, 2022 (156)
65	EVA	ss5843605017	Oct 13, 2022 (156)
66	EVA	ss5843605018	Oct 13, 2022 (156)
67	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 11102337 (NC_000004.11:15383045::AAA 744/3854) Row 11102338 (NC_000004.11:15383045::AA 307/3854)	-	Oct 12, 2018 (152)
68	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 11102337 (NC_000004.11:15383045::AAA 744/3854) Row 11102338 (NC_000004.11:15383045::AA 307/3854)	-	Oct 12, 2018 (152)
69	gnomAD - Genomes Submission ignored due to conflicting rows: Row 141323529 (NC_000004.12:15381421::A 21089/116458) Row 141323530 (NC_000004.12:15381421::AA 953/116618) Row 141323531 (NC_000004.12:15381421::AAA 26518/116210)...	-	Apr 26, 2021 (155)
70	gnomAD - Genomes Submission ignored due to conflicting rows: Row 141323529 (NC_000004.12:15381421::A 21089/116458) Row 141323530 (NC_000004.12:15381421::AA 953/116618) Row 141323531 (NC_000004.12:15381421::AAA 26518/116210)...	-	Apr 26, 2021 (155)
71	gnomAD - Genomes Submission ignored due to conflicting rows: Row 141323529 (NC_000004.12:15381421::A 21089/116458) Row 141323530 (NC_000004.12:15381421::AA 953/116618) Row 141323531 (NC_000004.12:15381421::AAA 26518/116210)...	-	Apr 26, 2021 (155)
72	gnomAD - Genomes Submission ignored due to conflicting rows: Row 141323529 (NC_000004.12:15381421::A 21089/116458) Row 141323530 (NC_000004.12:15381421::AA 953/116618) Row 141323531 (NC_000004.12:15381421::AAA 26518/116210)...	-	Apr 26, 2021 (155)
73	gnomAD - Genomes Submission ignored due to conflicting rows: Row 141323529 (NC_000004.12:15381421::A 21089/116458) Row 141323530 (NC_000004.12:15381421::AA 953/116618) Row 141323531 (NC_000004.12:15381421::AAA 26518/116210)...	-	Apr 26, 2021 (155)
74	gnomAD - Genomes Submission ignored due to conflicting rows: Row 141323529 (NC_000004.12:15381421::A 21089/116458) Row 141323530 (NC_000004.12:15381421::AA 953/116618) Row 141323531 (NC_000004.12:15381421::AAA 26518/116210)...	-	Apr 26, 2021 (155)
75	gnomAD - Genomes Submission ignored due to conflicting rows: Row 141323529 (NC_000004.12:15381421::A 21089/116458) Row 141323530 (NC_000004.12:15381421::AA 953/116618) Row 141323531 (NC_000004.12:15381421::AAA 26518/116210)...	-	Apr 26, 2021 (155)
76	Korean Genome Project Submission ignored due to conflicting rows: Row 9980330 (NC_000004.12:15381422::A 379/1816) Row 9980331 (NC_000004.12:15381422::AA 92/1816) Row 9980332 (NC_000004.12:15381421:A: 39/1816)...	-	Apr 26, 2020 (154)
77	Korean Genome Project Submission ignored due to conflicting rows: Row 9980330 (NC_000004.12:15381422::A 379/1816) Row 9980331 (NC_000004.12:15381422::AA 92/1816) Row 9980332 (NC_000004.12:15381421:A: 39/1816)...	-	Apr 26, 2020 (154)
78	Korean Genome Project Submission ignored due to conflicting rows: Row 9980330 (NC_000004.12:15381422::A 379/1816) Row 9980331 (NC_000004.12:15381422::AA 92/1816) Row 9980332 (NC_000004.12:15381421:A: 39/1816)...	-	Apr 26, 2020 (154)
79	Korean Genome Project Submission ignored due to conflicting rows: Row 9980330 (NC_000004.12:15381422::A 379/1816) Row 9980331 (NC_000004.12:15381422::AA 92/1816) Row 9980332 (NC_000004.12:15381421:A: 39/1816)...	-	Apr 26, 2020 (154)
80	Korean Genome Project Submission ignored due to conflicting rows: Row 9980330 (NC_000004.12:15381422::A 379/1816) Row 9980331 (NC_000004.12:15381422::AA 92/1816) Row 9980332 (NC_000004.12:15381421:A: 39/1816)...	-	Apr 26, 2020 (154)
81	Northern Sweden Submission ignored due to conflicting rows: Row 4174932 (NC_000004.11:15383045::AAA 95/500) Row 4174933 (NC_000004.11:15383045::A 61/500) Row 4174934 (NC_000004.11:15383045::AAAA 2/500)	-	Jul 13, 2019 (153)
82	Northern Sweden Submission ignored due to conflicting rows: Row 4174932 (NC_000004.11:15383045::AAA 95/500) Row 4174933 (NC_000004.11:15383045::A 61/500) Row 4174934 (NC_000004.11:15383045::AAAA 2/500)	-	Jul 13, 2019 (153)
83	Northern Sweden Submission ignored due to conflicting rows: Row 4174932 (NC_000004.11:15383045::AAA 95/500) Row 4174933 (NC_000004.11:15383045::A 61/500) Row 4174934 (NC_000004.11:15383045::AAAA 2/500)	-	Jul 13, 2019 (153)
84	8.3KJPN Submission ignored due to conflicting rows: Row 22342647 (NC_000004.11:15383045::A 4182/16730) Row 22342648 (NC_000004.11:15383045::AAA 5252/16730) Row 22342649 (NC_000004.11:15383045::AA 342/16730)...	-	Apr 26, 2021 (155)
85	8.3KJPN Submission ignored due to conflicting rows: Row 22342647 (NC_000004.11:15383045::A 4182/16730) Row 22342648 (NC_000004.11:15383045::AAA 5252/16730) Row 22342649 (NC_000004.11:15383045::AA 342/16730)...	-	Apr 26, 2021 (155)
86	8.3KJPN Submission ignored due to conflicting rows: Row 22342647 (NC_000004.11:15383045::A 4182/16730) Row 22342648 (NC_000004.11:15383045::AAA 5252/16730) Row 22342649 (NC_000004.11:15383045::AA 342/16730)...	-	Apr 26, 2021 (155)
87	8.3KJPN Submission ignored due to conflicting rows: Row 22342647 (NC_000004.11:15383045::A 4182/16730) Row 22342648 (NC_000004.11:15383045::AAA 5252/16730) Row 22342649 (NC_000004.11:15383045::AA 342/16730)...	-	Apr 26, 2021 (155)
88	8.3KJPN Submission ignored due to conflicting rows: Row 22342647 (NC_000004.11:15383045::A 4182/16730) Row 22342648 (NC_000004.11:15383045::AAA 5252/16730) Row 22342649 (NC_000004.11:15383045::AA 342/16730)...	-	Apr 26, 2021 (155)
89	14KJPN Submission ignored due to conflicting rows: Row 31907639 (NC_000004.12:15381421::A 6932/28258) Row 31907640 (NC_000004.12:15381421::AAA 9030/28258) Row 31907641 (NC_000004.12:15381421::AA 562/28258)...	-	Oct 13, 2022 (156)
90	14KJPN Submission ignored due to conflicting rows: Row 31907639 (NC_000004.12:15381421::A 6932/28258) Row 31907640 (NC_000004.12:15381421::AAA 9030/28258) Row 31907641 (NC_000004.12:15381421::AA 562/28258)...	-	Oct 13, 2022 (156)
91	14KJPN Submission ignored due to conflicting rows: Row 31907639 (NC_000004.12:15381421::A 6932/28258) Row 31907640 (NC_000004.12:15381421::AAA 9030/28258) Row 31907641 (NC_000004.12:15381421::AA 562/28258)...	-	Oct 13, 2022 (156)
92	14KJPN Submission ignored due to conflicting rows: Row 31907639 (NC_000004.12:15381421::A 6932/28258) Row 31907640 (NC_000004.12:15381421::AAA 9030/28258) Row 31907641 (NC_000004.12:15381421::AA 562/28258)...	-	Oct 13, 2022 (156)
93	14KJPN Submission ignored due to conflicting rows: Row 31907639 (NC_000004.12:15381421::A 6932/28258) Row 31907640 (NC_000004.12:15381421::AAA 9030/28258) Row 31907641 (NC_000004.12:15381421::AA 562/28258)...	-	Oct 13, 2022 (156)
94	UK 10K study - Twins Submission ignored due to conflicting rows: Row 11102337 (NC_000004.11:15383045::AAA 757/3708) Row 11102338 (NC_000004.11:15383045::AA 249/3708)	-	Oct 12, 2018 (152)
95	UK 10K study - Twins Submission ignored due to conflicting rows: Row 11102337 (NC_000004.11:15383045::AAA 757/3708) Row 11102338 (NC_000004.11:15383045::AA 249/3708)	-	Oct 12, 2018 (152)
96	ALFA	NC_000004.12 - 15381422	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)
rs376279757	May 15, 2013 (138)
rs58094912	May 11, 2012 (137)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4091208710, ss5258180567	NC_000004.12:15381421:AA:	NC_000004.12:15381421:AAAAAAAAAAAA… NC_000004.12:15381421:AAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
9262913375	NC_000004.12:15381421:AAAAAAAAAAAA… NC_000004.12:15381421:AAAAAAAAAAAAAAA:AAAAAAAAAAAAA	NC_000004.12:15381421:AAAAAAAAAAAA… NC_000004.12:15381421:AAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss82875088	NC_000004.9:15059328:A:	NC_000004.12:15381421:AAAAAAAAAAAA… NC_000004.12:15381421:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss3784630019, ss5164373344	NC_000004.11:15383045:A:	NC_000004.12:15381421:AAAAAAAAAAAA… NC_000004.12:15381421:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss3065934798, ss3711481854, ss3953602331, ss4091208709, ss5258180563, ss5457064569, ss5698070539	NC_000004.12:15381421:A:	NC_000004.12:15381421:AAAAAAAAAAAA… NC_000004.12:15381421:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
9262913375	NC_000004.12:15381421:AAAAAAAAAAAA… NC_000004.12:15381421:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	NC_000004.12:15381421:AAAAAAAAAAAA… NC_000004.12:15381421:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss288487418	NC_000004.10:14992158::A	NC_000004.12:15381421:AAAAAAAAAAAA… NC_000004.12:15381421:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss2994203461, ss3730890068, ss3828389898, ss5164373340	NC_000004.11:15383045::A	NC_000004.12:15381421:AAAAAAAAAAAA… NC_000004.12:15381421:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss4091208704, ss5258180564, ss5457064567, ss5698070535	NC_000004.12:15381421::A	NC_000004.12:15381421:AAAAAAAAAAAA… NC_000004.12:15381421:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
9262913375	NC_000004.12:15381421:AAAAAAAAAAAA… NC_000004.12:15381421:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	NC_000004.12:15381421:AAAAAAAAAAAA… NC_000004.12:15381421:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss3711481853, ss3953602329	NC_000004.12:15381422::A	NC_000004.12:15381421:AAAAAAAAAAAA… NC_000004.12:15381421:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss1704055389, ss1704055471, ss2625548807, ss5164373342, ss5843605018	NC_000004.11:15383045::AA	NC_000004.12:15381421:AAAAAAAAAAAA… NC_000004.12:15381421:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss4091208705, ss5258180566, ss5457064570, ss5698070537	NC_000004.12:15381421::AA	NC_000004.12:15381421:AAAAAAAAAAAA… NC_000004.12:15381421:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
9262913375	NC_000004.12:15381421:AAAAAAAAAAAA… NC_000004.12:15381421:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	NC_000004.12:15381421:AAAAAAAAAAAA… NC_000004.12:15381421:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss3711481852, ss3953602330	NC_000004.12:15381422::AA	NC_000004.12:15381421:AAAAAAAAAAAA… NC_000004.12:15381421:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss295153659	NC_000004.10:14992144::AAA	NC_000004.12:15381421:AAAAAAAAAAAA… NC_000004.12:15381421:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss295153660	NC_000004.10:14992156::AAA	NC_000004.12:15381421:AAAAAAAAAAAA… NC_000004.12:15381421:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss288487418	NC_000004.10:14992158::AAA	NC_000004.12:15381421:AAAAAAAAAAAA… NC_000004.12:15381421:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss663470258, ss666246597, ss1704055387, ss1704055468, ss2994203460, ss3730890067, ss3837628261, ss5164373341, ss5843605016	NC_000004.11:15383045::AAA	NC_000004.12:15381421:AAAAAAAAAAAA… NC_000004.12:15381421:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss3647661040, ss3843062435, ss4091208706, ss5258180562, ss5457064568, ss5698070536	NC_000004.12:15381421::AAA	NC_000004.12:15381421:AAAAAAAAAAAA… NC_000004.12:15381421:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
9262913375	NC_000004.12:15381421:AAAAAAAAAAAA… NC_000004.12:15381421:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	NC_000004.12:15381421:AAAAAAAAAAAA… NC_000004.12:15381421:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss3711481851, ss3953602332	NC_000004.12:15381422::AAA	NC_000004.12:15381421:AAAAAAAAAAAA… NC_000004.12:15381421:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss95346914	NT_006316.16:6564857::AAA	NC_000004.12:15381421:AAAAAAAAAAAA… NC_000004.12:15381421:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss2994203462, ss3730890069, ss5164373343, ss5843605017	NC_000004.11:15383045::AAAA	NC_000004.12:15381421:AAAAAAAAAAAA… NC_000004.12:15381421:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss4091208707, ss5258180565, ss5457064571, ss5698070538	NC_000004.12:15381421::AAAA	NC_000004.12:15381421:AAAAAAAAAAAA… NC_000004.12:15381421:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
9262913375	NC_000004.12:15381421:AAAAAAAAAAAA… NC_000004.12:15381421:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	NC_000004.12:15381421:AAAAAAAAAAAA… NC_000004.12:15381421:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss3711481850, ss3953602333	NC_000004.12:15381422::AAAA	NC_000004.12:15381421:AAAAAAAAAAAA… NC_000004.12:15381421:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss4091208708	NC_000004.12:15381421::AAAAA	NC_000004.12:15381421:AAAAAAAAAAAA… NC_000004.12:15381421:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss3711481849	NC_000004.12:15381422::AAAAAAAAAAA	NC_000004.12:15381421:AAAAAAAAAAAA… NC_000004.12:15381421:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	(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 rs11308911

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

rs11308911