Name: rs11361991
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.

rs11361991

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr6:116670371-116670389 (GRCh38.p14) Help
The anchor position for this RefSNP. Includes all nucleotides potentially affected by this change, thus it can differ from HGVS, which is right-shifted. See here for details.
Alleles: del(A)₁₃ / del(A)₁₁ / del(A)₉ / de…
del(A)₁₃ / del(A)₁₁ / del(A)₉ / del(A)₈ / del(A)₇ / del(A)₅ / del(A)₄ / delAAA / delAA / delA / dupA / dupAA / dupAAA / dup(A)₄ / dup(A)₅ / dup(A)₆ / dup(A)₇ / dup(A)₈ / dup(A)₉ / dup(A)₁₀ / dup(A)₁₂ / dup(A)₁₆ / dup(A)₁₇ / dup(A)₁₉
Variation Type: Indel Insertion and Deletion
Frequency: del(A)₈=0.1853 (714/3854, ALSPAC)
del(A)₁₃=0.0000 (0/3366, ALFA)
del(A)₁₁=0.0000 (0/3366, ALFA) (+ 10 more)
del(A)₉=0.0000 (0/3366, ALFA)
del(A)₈=0.0000 (0/3366, ALFA)
del(A)₇=0.0000 (0/3366, ALFA)
del(A)₅=0.0000 (0/3366, ALFA)
del(A)₄=0.0000 (0/3366, ALFA)
delAAA=0.0000 (0/3366, ALFA)
delAA=0.0000 (0/3366, ALFA)
delA=0.0000 (0/3366, ALFA)
dupA=0.0000 (0/3366, ALFA)
dupAA=0.0000 (0/3366, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: ZUP1 : 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	HWEP
Total	Global	3366	AAAAAAAAAAAAAAAAAAA=1.0000	AAAAAA=0.0000, AAAAAAAA=0.0000, AAAAAAAAAA=0.0000, AAAAAAAAAAA=0.0000, AAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAA=0.0000	1.0	N/A
European	Sub	1944	AAAAAAAAAAAAAAAAAAA=1.0000	AAAAAA=0.0000, AAAAAAAA=0.0000, AAAAAAAAAA=0.0000, AAAAAAAAAAA=0.0000, AAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAA=0.0000	1.0	N/A
African	Sub	988	AAAAAAAAAAAAAAAAAAA=1.000	AAAAAA=0.000, AAAAAAAA=0.000, AAAAAAAAAA=0.000, AAAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000	1.0	N/A
African Others	Sub	24	AAAAAAAAAAAAAAAAAAA=1.00	AAAAAA=0.00, AAAAAAAA=0.00, AAAAAAAAAA=0.00, AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
African American	Sub	964	AAAAAAAAAAAAAAAAAAA=1.000	AAAAAA=0.000, AAAAAAAA=0.000, AAAAAAAAAA=0.000, AAAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000	1.0	N/A
Asian	Sub	30	AAAAAAAAAAAAAAAAAAA=1.00	AAAAAA=0.00, AAAAAAAA=0.00, AAAAAAAAAA=0.00, AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
East Asian	Sub	18	AAAAAAAAAAAAAAAAAAA=1.00	AAAAAA=0.00, AAAAAAAA=0.00, AAAAAAAAAA=0.00, AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Other Asian	Sub	12	AAAAAAAAAAAAAAAAAAA=1.00	AAAAAA=0.00, AAAAAAAA=0.00, AAAAAAAAAA=0.00, AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Latin American 1	Sub	48	AAAAAAAAAAAAAAAAAAA=1.00	AAAAAA=0.00, AAAAAAAA=0.00, AAAAAAAAAA=0.00, AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Latin American 2	Sub	218	AAAAAAAAAAAAAAAAAAA=1.000	AAAAAA=0.000, AAAAAAAA=0.000, AAAAAAAAAA=0.000, AAAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000	1.0	N/A
South Asian	Sub	24	AAAAAAAAAAAAAAAAAAA=1.00	AAAAAA=0.00, AAAAAAAA=0.00, AAAAAAAAAA=0.00, AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Other	Sub	114	AAAAAAAAAAAAAAAAAAA=1.000	AAAAAA=0.000, AAAAAAAA=0.000, AAAAAAAAAA=0.000, AAAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=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
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	(A)₁₉=0.8147	del(A)₈=0.1853
Allele Frequency Aggregator	Total	Global	3366	(A)₁₉=1.0000	del(A)₁₃=0.0000, del(A)₁₁=0.0000, del(A)₉=0.0000, del(A)₈=0.0000, del(A)₇=0.0000, del(A)₅=0.0000, del(A)₄=0.0000, delAAA=0.0000, delAA=0.0000, delA=0.0000, dupA=0.0000, dupAA=0.0000
Allele Frequency Aggregator	European	Sub	1944	(A)₁₉=1.0000	del(A)₁₃=0.0000, del(A)₁₁=0.0000, del(A)₉=0.0000, del(A)₈=0.0000, del(A)₇=0.0000, del(A)₅=0.0000, del(A)₄=0.0000, delAAA=0.0000, delAA=0.0000, delA=0.0000, dupA=0.0000, dupAA=0.0000
Allele Frequency Aggregator	African	Sub	988	(A)₁₉=1.000	del(A)₁₃=0.000, del(A)₁₁=0.000, del(A)₉=0.000, del(A)₈=0.000, del(A)₇=0.000, del(A)₅=0.000, del(A)₄=0.000, delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000
Allele Frequency Aggregator	Latin American 2	Sub	218	(A)₁₉=1.000	del(A)₁₃=0.000, del(A)₁₁=0.000, del(A)₉=0.000, del(A)₈=0.000, del(A)₇=0.000, del(A)₅=0.000, del(A)₄=0.000, delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000
Allele Frequency Aggregator	Other	Sub	114	(A)₁₉=1.000	del(A)₁₃=0.000, del(A)₁₁=0.000, del(A)₉=0.000, del(A)₈=0.000, del(A)₇=0.000, del(A)₅=0.000, del(A)₄=0.000, delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000
Allele Frequency Aggregator	Latin American 1	Sub	48	(A)₁₉=1.00	del(A)₁₃=0.00, del(A)₁₁=0.00, del(A)₉=0.00, del(A)₈=0.00, del(A)₇=0.00, del(A)₅=0.00, del(A)₄=0.00, delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00
Allele Frequency Aggregator	Asian	Sub	30	(A)₁₉=1.00	del(A)₁₃=0.00, del(A)₁₁=0.00, del(A)₉=0.00, del(A)₈=0.00, del(A)₇=0.00, del(A)₅=0.00, del(A)₄=0.00, delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00
Allele Frequency Aggregator	South Asian	Sub	24	(A)₁₉=1.00	del(A)₁₃=0.00, del(A)₁₁=0.00, del(A)₉=0.00, del(A)₈=0.00, del(A)₇=0.00, del(A)₅=0.00, del(A)₄=0.00, delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=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 6	NC_000006.12:g.116670377_116670389del
GRCh38.p14 chr 6	NC_000006.12:g.116670379_116670389del
GRCh38.p14 chr 6	NC_000006.12:g.116670381_116670389del
GRCh38.p14 chr 6	NC_000006.12:g.116670382_116670389del
GRCh38.p14 chr 6	NC_000006.12:g.116670383_116670389del
GRCh38.p14 chr 6	NC_000006.12:g.116670385_116670389del
GRCh38.p14 chr 6	NC_000006.12:g.116670386_116670389del
GRCh38.p14 chr 6	NC_000006.12:g.116670387_116670389del
GRCh38.p14 chr 6	NC_000006.12:g.116670388_116670389del
GRCh38.p14 chr 6	NC_000006.12:g.116670389del
GRCh38.p14 chr 6	NC_000006.12:g.116670389dup
GRCh38.p14 chr 6	NC_000006.12:g.116670388_116670389dup
GRCh38.p14 chr 6	NC_000006.12:g.116670387_116670389dup
GRCh38.p14 chr 6	NC_000006.12:g.116670386_116670389dup
GRCh38.p14 chr 6	NC_000006.12:g.116670385_116670389dup
GRCh38.p14 chr 6	NC_000006.12:g.116670384_116670389dup
GRCh38.p14 chr 6	NC_000006.12:g.116670383_116670389dup
GRCh38.p14 chr 6	NC_000006.12:g.116670382_116670389dup
GRCh38.p14 chr 6	NC_000006.12:g.116670381_116670389dup
GRCh38.p14 chr 6	NC_000006.12:g.116670380_116670389dup
GRCh38.p14 chr 6	NC_000006.12:g.116670378_116670389dup
GRCh38.p14 chr 6	NC_000006.12:g.116670374_116670389dup
GRCh38.p14 chr 6	NC_000006.12:g.116670373_116670389dup
GRCh38.p14 chr 6	NC_000006.12:g.116670371_116670389dup
GRCh37.p13 chr 6	NC_000006.11:g.116991540_116991552del
GRCh37.p13 chr 6	NC_000006.11:g.116991542_116991552del
GRCh37.p13 chr 6	NC_000006.11:g.116991544_116991552del
GRCh37.p13 chr 6	NC_000006.11:g.116991545_116991552del
GRCh37.p13 chr 6	NC_000006.11:g.116991546_116991552del
GRCh37.p13 chr 6	NC_000006.11:g.116991548_116991552del
GRCh37.p13 chr 6	NC_000006.11:g.116991549_116991552del
GRCh37.p13 chr 6	NC_000006.11:g.116991550_116991552del
GRCh37.p13 chr 6	NC_000006.11:g.116991551_116991552del
GRCh37.p13 chr 6	NC_000006.11:g.116991552del
GRCh37.p13 chr 6	NC_000006.11:g.116991552dup
GRCh37.p13 chr 6	NC_000006.11:g.116991551_116991552dup
GRCh37.p13 chr 6	NC_000006.11:g.116991550_116991552dup
GRCh37.p13 chr 6	NC_000006.11:g.116991549_116991552dup
GRCh37.p13 chr 6	NC_000006.11:g.116991548_116991552dup
GRCh37.p13 chr 6	NC_000006.11:g.116991547_116991552dup
GRCh37.p13 chr 6	NC_000006.11:g.116991546_116991552dup
GRCh37.p13 chr 6	NC_000006.11:g.116991545_116991552dup
GRCh37.p13 chr 6	NC_000006.11:g.116991544_116991552dup
GRCh37.p13 chr 6	NC_000006.11:g.116991543_116991552dup
GRCh37.p13 chr 6	NC_000006.11:g.116991541_116991552dup
GRCh37.p13 chr 6	NC_000006.11:g.116991537_116991552dup
GRCh37.p13 chr 6	NC_000006.11:g.116991536_116991552dup
GRCh37.p13 chr 6	NC_000006.11:g.116991534_116991552dup

Gene: ZUP1, zinc finger containing ubiquitin peptidase 1 (minus strand) : 2KB Upstream Variant

Molecule type	Change	Amino acid[Codon]	SO Term
ZUP1 transcript variant 2	NM_001361189.2:c.	N/A	Upstream Transcript Variant
ZUP1 transcript variant 3	NM_001361190.2:c.	N/A	Upstream Transcript Variant
ZUP1 transcript variant 6	NM_001361191.2:c.	N/A	Upstream Transcript Variant
ZUP1 transcript variant 1	NM_145062.3:c.	N/A	Upstream Transcript Variant
ZUP1 transcript variant 4	NR_154586.2:n.	N/A	Upstream Transcript Variant
ZUP1 transcript variant 5	NR_154587.2:n.	N/A	Upstream Transcript Variant
ZUP1 transcript variant 7	NR_154588.2:n.	N/A	Upstream Transcript Variant
ZUP1 transcript variant 8	NR_154589.2: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	(A)₁₉=	del(A)₁₃	del(A)₁₁	del(A)₉	del(A)₈	del(A)₇	del(A)₅	del(A)₄	delAAA	delAA	delA	dupA	dupAA	dupAAA	dup(A)₄	dup(A)₅	dup(A)₆	dup(A)₇	dup(A)₈	dup(A)₉	dup(A)₁₀	dup(A)₁₂	dup(A)₁₆	dup(A)₁₇	dup(A)₁₉
GRCh38.p14 chr 6	NC_000006.12:g.116670371_116670389=	NC_000006.12:g.116670377_116670389del	NC_000006.12:g.116670379_116670389del	NC_000006.12:g.116670381_116670389del	NC_000006.12:g.116670382_116670389del	NC_000006.12:g.116670383_116670389del	NC_000006.12:g.116670385_116670389del	NC_000006.12:g.116670386_116670389del	NC_000006.12:g.116670387_116670389del	NC_000006.12:g.116670388_116670389del	NC_000006.12:g.116670389del	NC_000006.12:g.116670389dup	NC_000006.12:g.116670388_116670389dup	NC_000006.12:g.116670387_116670389dup	NC_000006.12:g.116670386_116670389dup	NC_000006.12:g.116670385_116670389dup	NC_000006.12:g.116670384_116670389dup	NC_000006.12:g.116670383_116670389dup	NC_000006.12:g.116670382_116670389dup	NC_000006.12:g.116670381_116670389dup	NC_000006.12:g.116670380_116670389dup	NC_000006.12:g.116670378_116670389dup	NC_000006.12:g.116670374_116670389dup	NC_000006.12:g.116670373_116670389dup	NC_000006.12:g.116670371_116670389dup
GRCh37.p13 chr 6	NC_000006.11:g.116991534_116991552=	NC_000006.11:g.116991540_116991552del	NC_000006.11:g.116991542_116991552del	NC_000006.11:g.116991544_116991552del	NC_000006.11:g.116991545_116991552del	NC_000006.11:g.116991546_116991552del	NC_000006.11:g.116991548_116991552del	NC_000006.11:g.116991549_116991552del	NC_000006.11:g.116991550_116991552del	NC_000006.11:g.116991551_116991552del	NC_000006.11:g.116991552del	NC_000006.11:g.116991552dup	NC_000006.11:g.116991551_116991552dup	NC_000006.11:g.116991550_116991552dup	NC_000006.11:g.116991549_116991552dup	NC_000006.11:g.116991548_116991552dup	NC_000006.11:g.116991547_116991552dup	NC_000006.11:g.116991546_116991552dup	NC_000006.11:g.116991545_116991552dup	NC_000006.11:g.116991544_116991552dup	NC_000006.11:g.116991543_116991552dup	NC_000006.11:g.116991541_116991552dup	NC_000006.11:g.116991537_116991552dup	NC_000006.11:g.116991536_116991552dup	NC_000006.11:g.116991534_116991552dup

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#.

63 SubSNP, 42 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	HUMANGENOME_JCVI	ss98460013	Dec 05, 2013 (138)
2	PJP	ss295303103	May 09, 2011 (137)
3	BILGI_BIOE	ss666371447	Apr 25, 2013 (138)
4	EVA_UK10K_ALSPAC	ss1705333129	Apr 01, 2015 (144)
5	EVA_UK10K_TWINSUK	ss1705333548	Apr 01, 2015 (144)
6	EVA_UK10K_ALSPAC	ss1710289979	Apr 01, 2015 (144)
7	EVA_UK10K_ALSPAC	ss1710289980	Apr 01, 2015 (144)
8	EVA_UK10K_TWINSUK	ss1710289995	Apr 01, 2015 (144)
9	EVA_UK10K_TWINSUK	ss1710289996	Apr 01, 2015 (144)
10	SWEGEN	ss2999814851	Nov 08, 2017 (151)
11	EVA_DECODE	ss3718110935	Jul 13, 2019 (153)
12	EVA_DECODE	ss3718110936	Jul 13, 2019 (153)
13	EVA_DECODE	ss3718110937	Jul 13, 2019 (153)
14	EVA_DECODE	ss3718110938	Jul 13, 2019 (153)
15	EVA_DECODE	ss3718110939	Jul 13, 2019 (153)
16	EVA_DECODE	ss3718110940	Jul 13, 2019 (153)
17	ACPOP	ss3733907430	Jul 13, 2019 (153)
18	ACPOP	ss3733907431	Jul 13, 2019 (153)
19	ACPOP	ss3733907432	Jul 13, 2019 (153)
20	EVA	ss3830152986	Apr 26, 2020 (154)
21	KOGIC	ss3959920614	Apr 26, 2020 (154)
22	KOGIC	ss3959920615	Apr 26, 2020 (154)
23	KOGIC	ss3959920616	Apr 26, 2020 (154)
24	KOGIC	ss3959920617	Apr 26, 2020 (154)
25	GNOMAD	ss4149908059	Apr 26, 2021 (155)
26	GNOMAD	ss4149908060	Apr 26, 2021 (155)
27	GNOMAD	ss4149908061	Apr 26, 2021 (155)
28	GNOMAD	ss4149908062	Apr 26, 2021 (155)
29	GNOMAD	ss4149908063	Apr 26, 2021 (155)
30	GNOMAD	ss4149908064	Apr 26, 2021 (155)
31	GNOMAD	ss4149908065	Apr 26, 2021 (155)
32	GNOMAD	ss4149908066	Apr 26, 2021 (155)
33	GNOMAD	ss4149908067	Apr 26, 2021 (155)
34	GNOMAD	ss4149908068	Apr 26, 2021 (155)
35	GNOMAD	ss4149908069	Apr 26, 2021 (155)
36	GNOMAD	ss4149908070	Apr 26, 2021 (155)
37	GNOMAD	ss4149908071	Apr 26, 2021 (155)
38	GNOMAD	ss4149908072	Apr 26, 2021 (155)
39	GNOMAD	ss4149908073	Apr 26, 2021 (155)
40	GNOMAD	ss4149908074	Apr 26, 2021 (155)
41	GNOMAD	ss4149908075	Apr 26, 2021 (155)
42	GNOMAD	ss4149908076	Apr 26, 2021 (155)
43	GNOMAD	ss4149908077	Apr 26, 2021 (155)
44	GNOMAD	ss4149908078	Apr 26, 2021 (155)
45	TOMMO_GENOMICS	ss5179547392	Apr 26, 2021 (155)
46	TOMMO_GENOMICS	ss5179547393	Apr 26, 2021 (155)
47	TOMMO_GENOMICS	ss5179547394	Apr 26, 2021 (155)
48	TOMMO_GENOMICS	ss5179547395	Apr 26, 2021 (155)
49	1000G_HIGH_COVERAGE	ss5270050320	Oct 13, 2022 (156)
50	1000G_HIGH_COVERAGE	ss5270050321	Oct 13, 2022 (156)
51	1000G_HIGH_COVERAGE	ss5270050322	Oct 13, 2022 (156)
52	1000G_HIGH_COVERAGE	ss5270050323	Oct 13, 2022 (156)
53	1000G_HIGH_COVERAGE	ss5270050325	Oct 13, 2022 (156)
54	HUGCELL_USP	ss5467520341	Oct 13, 2022 (156)
55	HUGCELL_USP	ss5467520342	Oct 13, 2022 (156)
56	HUGCELL_USP	ss5467520343	Oct 13, 2022 (156)
57	HUGCELL_USP	ss5467520344	Oct 13, 2022 (156)
58	TOMMO_GENOMICS	ss5718327380	Oct 13, 2022 (156)
59	TOMMO_GENOMICS	ss5718327381	Oct 13, 2022 (156)
60	TOMMO_GENOMICS	ss5718327382	Oct 13, 2022 (156)
61	TOMMO_GENOMICS	ss5718327383	Oct 13, 2022 (156)
62	TOMMO_GENOMICS	ss5718327384	Oct 13, 2022 (156)
63	EVA	ss5855547575	Oct 13, 2022 (156)
64	The Avon Longitudinal Study of Parents and Children	NC_000006.11 - 116991534	Oct 12, 2018 (152)
65	gnomAD - Genomes Submission ignored due to conflicting rows: Row 238597259 (NC_000006.12:116670370::A 143/84204) Row 238597260 (NC_000006.12:116670370::AA 442/84184) Row 238597261 (NC_000006.12:116670370::AAA 12/84250)...	-	Apr 26, 2021 (155)
66	gnomAD - Genomes Submission ignored due to conflicting rows: Row 238597259 (NC_000006.12:116670370::A 143/84204) Row 238597260 (NC_000006.12:116670370::AA 442/84184) Row 238597261 (NC_000006.12:116670370::AAA 12/84250)...	-	Apr 26, 2021 (155)
67	gnomAD - Genomes Submission ignored due to conflicting rows: Row 238597259 (NC_000006.12:116670370::A 143/84204) Row 238597260 (NC_000006.12:116670370::AA 442/84184) Row 238597261 (NC_000006.12:116670370::AAA 12/84250)...	-	Apr 26, 2021 (155)
68	gnomAD - Genomes Submission ignored due to conflicting rows: Row 238597259 (NC_000006.12:116670370::A 143/84204) Row 238597260 (NC_000006.12:116670370::AA 442/84184) Row 238597261 (NC_000006.12:116670370::AAA 12/84250)...	-	Apr 26, 2021 (155)
69	gnomAD - Genomes Submission ignored due to conflicting rows: Row 238597259 (NC_000006.12:116670370::A 143/84204) Row 238597260 (NC_000006.12:116670370::AA 442/84184) Row 238597261 (NC_000006.12:116670370::AAA 12/84250)...	-	Apr 26, 2021 (155)
70	gnomAD - Genomes Submission ignored due to conflicting rows: Row 238597259 (NC_000006.12:116670370::A 143/84204) Row 238597260 (NC_000006.12:116670370::AA 442/84184) Row 238597261 (NC_000006.12:116670370::AAA 12/84250)...	-	Apr 26, 2021 (155)
71	gnomAD - Genomes Submission ignored due to conflicting rows: Row 238597259 (NC_000006.12:116670370::A 143/84204) Row 238597260 (NC_000006.12:116670370::AA 442/84184) Row 238597261 (NC_000006.12:116670370::AAA 12/84250)...	-	Apr 26, 2021 (155)
72	gnomAD - Genomes Submission ignored due to conflicting rows: Row 238597259 (NC_000006.12:116670370::A 143/84204) Row 238597260 (NC_000006.12:116670370::AA 442/84184) Row 238597261 (NC_000006.12:116670370::AAA 12/84250)...	-	Apr 26, 2021 (155)
73	gnomAD - Genomes Submission ignored due to conflicting rows: Row 238597259 (NC_000006.12:116670370::A 143/84204) Row 238597260 (NC_000006.12:116670370::AA 442/84184) Row 238597261 (NC_000006.12:116670370::AAA 12/84250)...	-	Apr 26, 2021 (155)
74	gnomAD - Genomes Submission ignored due to conflicting rows: Row 238597259 (NC_000006.12:116670370::A 143/84204) Row 238597260 (NC_000006.12:116670370::AA 442/84184) Row 238597261 (NC_000006.12:116670370::AAA 12/84250)...	-	Apr 26, 2021 (155)
75	gnomAD - Genomes Submission ignored due to conflicting rows: Row 238597259 (NC_000006.12:116670370::A 143/84204) Row 238597260 (NC_000006.12:116670370::AA 442/84184) Row 238597261 (NC_000006.12:116670370::AAA 12/84250)...	-	Apr 26, 2021 (155)
76	gnomAD - Genomes Submission ignored due to conflicting rows: Row 238597259 (NC_000006.12:116670370::A 143/84204) Row 238597260 (NC_000006.12:116670370::AA 442/84184) Row 238597261 (NC_000006.12:116670370::AAA 12/84250)...	-	Apr 26, 2021 (155)
77	gnomAD - Genomes Submission ignored due to conflicting rows: Row 238597259 (NC_000006.12:116670370::A 143/84204) Row 238597260 (NC_000006.12:116670370::AA 442/84184) Row 238597261 (NC_000006.12:116670370::AAA 12/84250)...	-	Apr 26, 2021 (155)
78	gnomAD - Genomes Submission ignored due to conflicting rows: Row 238597259 (NC_000006.12:116670370::A 143/84204) Row 238597260 (NC_000006.12:116670370::AA 442/84184) Row 238597261 (NC_000006.12:116670370::AAA 12/84250)...	-	Apr 26, 2021 (155)
79	gnomAD - Genomes Submission ignored due to conflicting rows: Row 238597259 (NC_000006.12:116670370::A 143/84204) Row 238597260 (NC_000006.12:116670370::AA 442/84184) Row 238597261 (NC_000006.12:116670370::AAA 12/84250)...	-	Apr 26, 2021 (155)
80	gnomAD - Genomes Submission ignored due to conflicting rows: Row 238597259 (NC_000006.12:116670370::A 143/84204) Row 238597260 (NC_000006.12:116670370::AA 442/84184) Row 238597261 (NC_000006.12:116670370::AAA 12/84250)...	-	Apr 26, 2021 (155)
81	gnomAD - Genomes Submission ignored due to conflicting rows: Row 238597259 (NC_000006.12:116670370::A 143/84204) Row 238597260 (NC_000006.12:116670370::AA 442/84184) Row 238597261 (NC_000006.12:116670370::AAA 12/84250)...	-	Apr 26, 2021 (155)
82	gnomAD - Genomes Submission ignored due to conflicting rows: Row 238597259 (NC_000006.12:116670370::A 143/84204) Row 238597260 (NC_000006.12:116670370::AA 442/84184) Row 238597261 (NC_000006.12:116670370::AAA 12/84250)...	-	Apr 26, 2021 (155)
83	gnomAD - Genomes Submission ignored due to conflicting rows: Row 238597259 (NC_000006.12:116670370::A 143/84204) Row 238597260 (NC_000006.12:116670370::AA 442/84184) Row 238597261 (NC_000006.12:116670370::AAA 12/84250)...	-	Apr 26, 2021 (155)
84	gnomAD - Genomes Submission ignored due to conflicting rows: Row 238597259 (NC_000006.12:116670370::A 143/84204) Row 238597260 (NC_000006.12:116670370::AA 442/84184) Row 238597261 (NC_000006.12:116670370::AAA 12/84250)...	-	Apr 26, 2021 (155)
85	gnomAD - Genomes Submission ignored due to conflicting rows: Row 238597259 (NC_000006.12:116670370::A 143/84204) Row 238597260 (NC_000006.12:116670370::AA 442/84184) Row 238597261 (NC_000006.12:116670370::AAA 12/84250)...	-	Apr 26, 2021 (155)
86	Korean Genome Project Submission ignored due to conflicting rows: Row 16298615 (NC_000006.12:116670376:AA: 107/1778) Row 16298616 (NC_000006.12:116670377:A: 831/1778) Row 16298617 (NC_000006.12:116670378::A 15/1778)...	-	Apr 26, 2020 (154)
87	Korean Genome Project Submission ignored due to conflicting rows: Row 16298615 (NC_000006.12:116670376:AA: 107/1778) Row 16298616 (NC_000006.12:116670377:A: 831/1778) Row 16298617 (NC_000006.12:116670378::A 15/1778)...	-	Apr 26, 2020 (154)
88	Korean Genome Project Submission ignored due to conflicting rows: Row 16298615 (NC_000006.12:116670376:AA: 107/1778) Row 16298616 (NC_000006.12:116670377:A: 831/1778) Row 16298617 (NC_000006.12:116670378::A 15/1778)...	-	Apr 26, 2020 (154)
89	Korean Genome Project Submission ignored due to conflicting rows: Row 16298615 (NC_000006.12:116670376:AA: 107/1778) Row 16298616 (NC_000006.12:116670377:A: 831/1778) Row 16298617 (NC_000006.12:116670378::A 15/1778)...	-	Apr 26, 2020 (154)
90	Northern Sweden Submission ignored due to conflicting rows: Row 7192295 (NC_000006.11:116991533:A: 86/518) Row 7192296 (NC_000006.11:116991533:AAAAAAAA: 73/518) Row 7192297 (NC_000006.11:116991533::AAAA 8/518)	-	Jul 13, 2019 (153)
91	Northern Sweden Submission ignored due to conflicting rows: Row 7192295 (NC_000006.11:116991533:A: 86/518) Row 7192296 (NC_000006.11:116991533:AAAAAAAA: 73/518) Row 7192297 (NC_000006.11:116991533::AAAA 8/518)	-	Jul 13, 2019 (153)
92	Northern Sweden Submission ignored due to conflicting rows: Row 7192295 (NC_000006.11:116991533:A: 86/518) Row 7192296 (NC_000006.11:116991533:AAAAAAAA: 73/518) Row 7192297 (NC_000006.11:116991533::AAAA 8/518)	-	Jul 13, 2019 (153)
93	8.3KJPN Submission ignored due to conflicting rows: Row 37516699 (NC_000006.11:116991533:A: 8017/16490) Row 37516700 (NC_000006.11:116991533:AA: 290/16490) Row 37516701 (NC_000006.11:116991533::A 48/16490)...	-	Apr 26, 2021 (155)
94	8.3KJPN Submission ignored due to conflicting rows: Row 37516699 (NC_000006.11:116991533:A: 8017/16490) Row 37516700 (NC_000006.11:116991533:AA: 290/16490) Row 37516701 (NC_000006.11:116991533::A 48/16490)...	-	Apr 26, 2021 (155)
95	8.3KJPN Submission ignored due to conflicting rows: Row 37516699 (NC_000006.11:116991533:A: 8017/16490) Row 37516700 (NC_000006.11:116991533:AA: 290/16490) Row 37516701 (NC_000006.11:116991533::A 48/16490)...	-	Apr 26, 2021 (155)
96	8.3KJPN Submission ignored due to conflicting rows: Row 37516699 (NC_000006.11:116991533:A: 8017/16490) Row 37516700 (NC_000006.11:116991533:AA: 290/16490) Row 37516701 (NC_000006.11:116991533::A 48/16490)...	-	Apr 26, 2021 (155)
97	14KJPN Submission ignored due to conflicting rows: Row 52164484 (NC_000006.12:116670370:A: 13416/27772) Row 52164485 (NC_000006.12:116670370:AAAAA: 61/27772) Row 52164486 (NC_000006.12:116670370:AA: 462/27772)...	-	Oct 13, 2022 (156)
98	14KJPN Submission ignored due to conflicting rows: Row 52164484 (NC_000006.12:116670370:A: 13416/27772) Row 52164485 (NC_000006.12:116670370:AAAAA: 61/27772) Row 52164486 (NC_000006.12:116670370:AA: 462/27772)...	-	Oct 13, 2022 (156)
99	14KJPN Submission ignored due to conflicting rows: Row 52164484 (NC_000006.12:116670370:A: 13416/27772) Row 52164485 (NC_000006.12:116670370:AAAAA: 61/27772) Row 52164486 (NC_000006.12:116670370:AA: 462/27772)...	-	Oct 13, 2022 (156)
100	14KJPN Submission ignored due to conflicting rows: Row 52164484 (NC_000006.12:116670370:A: 13416/27772) Row 52164485 (NC_000006.12:116670370:AAAAA: 61/27772) Row 52164486 (NC_000006.12:116670370:AA: 462/27772)...	-	Oct 13, 2022 (156)
101	14KJPN Submission ignored due to conflicting rows: Row 52164484 (NC_000006.12:116670370:A: 13416/27772) Row 52164485 (NC_000006.12:116670370:AAAAA: 61/27772) Row 52164486 (NC_000006.12:116670370:AA: 462/27772)...	-	Oct 13, 2022 (156)
102	UK 10K study - Twins Submission ignored due to conflicting rows: Row 18828032 (NC_000006.11:116991540:A: 1707/3708) Row 18828033 (NC_000006.11:116991533:AAAAAAAA: 649/3708) Row 18828034 (NC_000006.11:116991539:AA: 807/3708)	-	Apr 26, 2020 (154)
103	UK 10K study - Twins	-	Oct 12, 2018 (152)
104	UK 10K study - Twins Submission ignored due to conflicting rows: Row 18828032 (NC_000006.11:116991540:A: 1707/3708) Row 18828033 (NC_000006.11:116991533:AAAAAAAA: 649/3708) Row 18828034 (NC_000006.11:116991539:AA: 807/3708)	-	Apr 26, 2020 (154)
105	ALFA	NC_000006.12 - 116670371	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)
rs71554857	May 11, 2012 (137)
rs71758374	May 11, 2012 (137)
rs147690044	May 11, 2012 (137)
rs375612480	May 13, 2013 (138)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
8025560093	NC_000006.12:116670370:AAAAAAAAAAA… NC_000006.12:116670370:AAAAAAAAAAAAAAAAAAA:AAAAAA	NC_000006.12:116670370:AAAAAAAAAAA… NC_000006.12:116670370:AAAAAAAAAAAAAAAAAAA:AAAAAA	(self)
8025560093	NC_000006.12:116670370:AAAAAAAAAAA… NC_000006.12:116670370:AAAAAAAAAAAAAAAAAAA:AAAAAAAA	NC_000006.12:116670370:AAAAAAAAAAA… NC_000006.12:116670370:AAAAAAAAAAAAAAAAAAA:AAAAAAAA	(self)
ss4149908078	NC_000006.12:116670370:AAAAAAAAA:	NC_000006.12:116670370:AAAAAAAAAAA… NC_000006.12:116670370:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAA	(self)
8025560093	NC_000006.12:116670370:AAAAAAAAAAA… NC_000006.12:116670370:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAA	NC_000006.12:116670370:AAAAAAAAAAA… NC_000006.12:116670370:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAA	(self)
18828033, ss1705333129, ss1705333548, ss2999814851, ss3733907431	NC_000006.11:116991533:AAAAAAAA:	NC_000006.12:116670370:AAAAAAAAAAA… NC_000006.12:116670370:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA	(self)
ss3718110940, ss3959920617, ss4149908077, ss5270050323, ss5467520343	NC_000006.12:116670370:AAAAAAAA:	NC_000006.12:116670370:AAAAAAAAAAA… NC_000006.12:116670370:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA	(self)
8025560093	NC_000006.12:116670370:AAAAAAAAAAA… NC_000006.12:116670370:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA	NC_000006.12:116670370:AAAAAAAAAAA… NC_000006.12:116670370:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA	(self)
ss4149908076	NC_000006.12:116670370:AAAAAAA:	NC_000006.12:116670370:AAAAAAAAAAA… NC_000006.12:116670370:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
8025560093	NC_000006.12:116670370:AAAAAAAAAAA… NC_000006.12:116670370:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	NC_000006.12:116670370:AAAAAAAAAAA… NC_000006.12:116670370:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
ss4149908075, ss5270050321, ss5718327381	NC_000006.12:116670370:AAAAA:	NC_000006.12:116670370:AAAAAAAAAAA… NC_000006.12:116670370:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
8025560093	NC_000006.12:116670370:AAAAAAAAAAA… NC_000006.12:116670370:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	NC_000006.12:116670370:AAAAAAAAAAA… NC_000006.12:116670370:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
8025560093	NC_000006.12:116670370:AAAAAAAAAAA… NC_000006.12:116670370:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	NC_000006.12:116670370:AAAAAAAAAAA… NC_000006.12:116670370:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss4149908074	NC_000006.12:116670370:AAA:	NC_000006.12:116670370:AAAAAAAAAAA… NC_000006.12:116670370:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
8025560093	NC_000006.12:116670370:AAAAAAAAAAA… NC_000006.12:116670370:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	NC_000006.12:116670370:AAAAAAAAAAA… NC_000006.12:116670370:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss3718110939	NC_000006.12:116670375:AAA:	NC_000006.12:116670370:AAAAAAAAAAA… NC_000006.12:116670370:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss5179547393	NC_000006.11:116991533:AA:	NC_000006.12:116670370:AAAAAAAAAAA… NC_000006.12:116670370:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss1710289980, ss1710289996	NC_000006.11:116991539:AA:	NC_000006.12:116670370:AAAAAAAAAAA… NC_000006.12:116670370:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss4149908073, ss5270050325, ss5467520341, ss5718327382	NC_000006.12:116670370:AA:	NC_000006.12:116670370:AAAAAAAAAAA… NC_000006.12:116670370:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
8025560093	NC_000006.12:116670370:AAAAAAAAAAA… NC_000006.12:116670370:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	NC_000006.12:116670370:AAAAAAAAAAA… NC_000006.12:116670370:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss3718110938, ss3959920614	NC_000006.12:116670376:AA:	NC_000006.12:116670370:AAAAAAAAAAA… NC_000006.12:116670370:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss295303103	NC_000006.10:117098226:A:	NC_000006.12:116670370:AAAAAAAAAAA… NC_000006.12:116670370:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss666371447, ss3733907430, ss3830152986, ss5179547392	NC_000006.11:116991533:A:	NC_000006.12:116670370:AAAAAAAAAAA… NC_000006.12:116670370:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss1710289979, ss1710289995	NC_000006.11:116991540:A:	NC_000006.12:116670370:AAAAAAAAAAA… NC_000006.12:116670370:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss5270050320, ss5467520342, ss5718327380, ss5855547575	NC_000006.12:116670370:A:	NC_000006.12:116670370:AAAAAAAAAAA… NC_000006.12:116670370:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
8025560093	NC_000006.12:116670370:AAAAAAAAAAA… NC_000006.12:116670370:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	NC_000006.12:116670370:AAAAAAAAAAA… NC_000006.12:116670370:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss3718110937, ss3959920615	NC_000006.12:116670377:A:	NC_000006.12:116670370:AAAAAAAAAAA… NC_000006.12:116670370:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss98460013	NT_025741.15:21161008:A:	NC_000006.12:116670370:AAAAAAAAAAA… NC_000006.12:116670370:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss5179547394	NC_000006.11:116991533::A	NC_000006.12:116670370:AAAAAAAAAAA… NC_000006.12:116670370:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss4149908059, ss5270050322, ss5467520344, ss5718327384	NC_000006.12:116670370::A	NC_000006.12:116670370:AAAAAAAAAAA… NC_000006.12:116670370:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
8025560093	NC_000006.12:116670370:AAAAAAAAAAA… NC_000006.12:116670370:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	NC_000006.12:116670370:AAAAAAAAAAA… NC_000006.12:116670370:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss3718110936, ss3959920616	NC_000006.12:116670378::A	NC_000006.12:116670370:AAAAAAAAAAA… NC_000006.12:116670370:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss4149908060	NC_000006.12:116670370::AA	NC_000006.12:116670370:AAAAAAAAAAA… NC_000006.12:116670370:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
8025560093	NC_000006.12:116670370:AAAAAAAAAAA… NC_000006.12:116670370:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	NC_000006.12:116670370:AAAAAAAAAAA… NC_000006.12:116670370:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
ss4149908061, ss5718327383	NC_000006.12:116670370::AAA	NC_000006.12:116670370:AAAAAAAAAAA… NC_000006.12:116670370:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
ss3718110935	NC_000006.12:116670378::AAA	NC_000006.12:116670370:AAAAAAAAAAA… NC_000006.12:116670370:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
ss3733907432	NC_000006.11:116991533::AAAA	NC_000006.12:116670370:AAAAAAAAAAA… NC_000006.12:116670370:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4149908062	NC_000006.12:116670370::AAAA	NC_000006.12:116670370:AAAAAAAAAAA… NC_000006.12:116670370:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4149908063	NC_000006.12:116670370::AAAAA	NC_000006.12:116670370:AAAAAAAAAAA… NC_000006.12:116670370:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4149908064	NC_000006.12:116670370::AAAAAA	NC_000006.12:116670370:AAAAAAAAAAA… NC_000006.12:116670370:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4149908065	NC_000006.12:116670370::AAAAAAA	NC_000006.12:116670370:AAAAAAAAAAA… NC_000006.12:116670370:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4149908066	NC_000006.12:116670370::AAAAAAAA	NC_000006.12:116670370:AAAAAAAAAAA… NC_000006.12:116670370:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4149908067	NC_000006.12:116670370::AAAAAAAAA	NC_000006.12:116670370:AAAAAAAAAAA… NC_000006.12:116670370:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4149908068	NC_000006.12:116670370::AAAAAAAAAA	NC_000006.12:116670370:AAAAAAAAAAA… NC_000006.12:116670370:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4149908069	NC_000006.12:116670370::AAAAAAAAAA… NC_000006.12:116670370::AAAAAAAAAAAA	NC_000006.12:116670370:AAAAAAAAAAA… NC_000006.12:116670370:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4149908070	NC_000006.12:116670370::AAAAAAAAAA… NC_000006.12:116670370::AAAAAAAAAAAAAAAA	NC_000006.12:116670370:AAAAAAAAAAA… NC_000006.12:116670370:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss5179547395	NC_000006.11:116991533::AAAAAAAAAA… NC_000006.11:116991533::AAAAAAAAAAAAAAAAA	NC_000006.12:116670370:AAAAAAAAAAA… NC_000006.12:116670370:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4149908071	NC_000006.12:116670370::AAAAAAAAAA… NC_000006.12:116670370::AAAAAAAAAAAAAAAAA	NC_000006.12:116670370:AAAAAAAAAAA… NC_000006.12:116670370:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4149908072	NC_000006.12:116670370::AAAAAAAAAA… NC_000006.12:116670370::AAAAAAAAAAAAAAAAAAA	NC_000006.12:116670370:AAAAAAAAAAA… NC_000006.12:116670370:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)

Removed from this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Destination RSIDs
ss3509633688	NC_000006.12:116670370:AAAAAAAAAAA:	NC_000006.12:116670370:AAAAAAAAAAA… NC_000006.12:116670370:AAAAAAAAAAAAAAAAAAA:AAAAAAAA

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

No publications for rs11361991

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.

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dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs11361991