Name: rs11451861
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.

rs11451861

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr1:71180877-71180901 (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)₁₄ / del(A)₁₃ / del(A)₁₁ / d…
del(A)₁₄ / del(A)₁₃ / del(A)₁₁ / del(A)₈ / del(A)₆ / 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)₁₁ / dup(A)₁₃ / ins(A)₂₈ / ins(A)₃₂
Variation Type: Indel Insertion and Deletion
Frequency: del(A)₈=0.000174 (46/264690, TOPMED)
del(A)₁₄=0.0000 (0/3194, ALFA)
del(A)₁₃=0.0000 (0/3194, ALFA) (+ 11 more)
del(A)₁₁=0.0000 (0/3194, ALFA)
del(A)₈=0.0000 (0/3194, ALFA)
del(A)₆=0.0000 (0/3194, ALFA)
del(A)₄=0.0000 (0/3194, ALFA)
delAAA=0.0000 (0/3194, ALFA)
delAA=0.0000 (0/3194, ALFA)
delA=0.0000 (0/3194, ALFA)
dupA=0.0000 (0/3194, ALFA)
dupAA=0.0000 (0/3194, ALFA)
dupAAA=0.0000 (0/3194, ALFA)
dup(A)₄=0.0000 (0/3194, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: ZRANB2-DT : 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	3194	AAAAAAAAAAAAAAAAAAAAAAAAA=1.0000	AAAAAAAAAAA=0.0000, AAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000	1.0	N/A
European	Sub	2110	AAAAAAAAAAAAAAAAAAAAAAAAA=1.0000	AAAAAAAAAAA=0.0000, AAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000	1.0	N/A
African	Sub	568	AAAAAAAAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	N/A
African Others	Sub	20	AAAAAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
African American	Sub	548	AAAAAAAAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	N/A
Asian	Sub	46	AAAAAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
East Asian	Sub	42	AAAAAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Other Asian	Sub	4	AAAAAAAAAAAAAAAAAAAAAAAAA=1.0	AAAAAAAAAAA=0.0, AAAAAAAAAAAA=0.0, AAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0	1.0	N/A
Latin American 1	Sub	46	AAAAAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Latin American 2	Sub	268	AAAAAAAAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	N/A
South Asian	Sub	26	AAAAAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Other	Sub	130	AAAAAAAAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=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").

Download

Study	Population	Group	Sample Size	Ref Allele	Alt Allele
TopMed	Global	Study-wide	264690	(A)₂₅=0.999826	del(A)₈=0.000174
Allele Frequency Aggregator	Total	Global	3194	(A)₂₅=1.0000	del(A)₁₄=0.0000, del(A)₁₃=0.0000, del(A)₁₁=0.0000, del(A)₈=0.0000, del(A)₆=0.0000, del(A)₄=0.0000, delAAA=0.0000, 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	2110	(A)₂₅=1.0000	del(A)₁₄=0.0000, del(A)₁₃=0.0000, del(A)₁₁=0.0000, del(A)₈=0.0000, del(A)₆=0.0000, del(A)₄=0.0000, delAAA=0.0000, 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	568	(A)₂₅=1.000	del(A)₁₄=0.000, del(A)₁₃=0.000, del(A)₁₁=0.000, del(A)₈=0.000, del(A)₆=0.000, del(A)₄=0.000, delAAA=0.000, 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	268	(A)₂₅=1.000	del(A)₁₄=0.000, del(A)₁₃=0.000, del(A)₁₁=0.000, del(A)₈=0.000, del(A)₆=0.000, del(A)₄=0.000, delAAA=0.000, 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	130	(A)₂₅=1.000	del(A)₁₄=0.000, del(A)₁₃=0.000, del(A)₁₁=0.000, del(A)₈=0.000, del(A)₆=0.000, del(A)₄=0.000, delAAA=0.000, 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	46	(A)₂₅=1.00	del(A)₁₄=0.00, del(A)₁₃=0.00, del(A)₁₁=0.00, del(A)₈=0.00, del(A)₆=0.00, del(A)₄=0.00, delAAA=0.00, 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	46	(A)₂₅=1.00	del(A)₁₄=0.00, del(A)₁₃=0.00, del(A)₁₁=0.00, del(A)₈=0.00, del(A)₆=0.00, del(A)₄=0.00, delAAA=0.00, 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	26	(A)₂₅=1.00	del(A)₁₄=0.00, del(A)₁₃=0.00, del(A)₁₁=0.00, del(A)₈=0.00, del(A)₆=0.00, del(A)₄=0.00, delAAA=0.00, 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 1	NC_000001.11:g.71180888_71180901del
GRCh38.p14 chr 1	NC_000001.11:g.71180889_71180901del
GRCh38.p14 chr 1	NC_000001.11:g.71180891_71180901del
GRCh38.p14 chr 1	NC_000001.11:g.71180894_71180901del
GRCh38.p14 chr 1	NC_000001.11:g.71180896_71180901del
GRCh38.p14 chr 1	NC_000001.11:g.71180898_71180901del
GRCh38.p14 chr 1	NC_000001.11:g.71180899_71180901del
GRCh38.p14 chr 1	NC_000001.11:g.71180900_71180901del
GRCh38.p14 chr 1	NC_000001.11:g.71180901del
GRCh38.p14 chr 1	NC_000001.11:g.71180901dup
GRCh38.p14 chr 1	NC_000001.11:g.71180900_71180901dup
GRCh38.p14 chr 1	NC_000001.11:g.71180899_71180901dup
GRCh38.p14 chr 1	NC_000001.11:g.71180898_71180901dup
GRCh38.p14 chr 1	NC_000001.11:g.71180897_71180901dup
GRCh38.p14 chr 1	NC_000001.11:g.71180896_71180901dup
GRCh38.p14 chr 1	NC_000001.11:g.71180895_71180901dup
GRCh38.p14 chr 1	NC_000001.11:g.71180894_71180901dup
GRCh38.p14 chr 1	NC_000001.11:g.71180893_71180901dup
GRCh38.p14 chr 1	NC_000001.11:g.71180892_71180901dup
GRCh38.p14 chr 1	NC_000001.11:g.71180891_71180901dup
GRCh38.p14 chr 1	NC_000001.11:g.71180889_71180901dup
GRCh38.p14 chr 1	NC_000001.11:g.71180901_71180902insAAAAAAAAAAAAAAAAAAAAAAAAAAAA
GRCh38.p14 chr 1	NC_000001.11:g.71180901_71180902insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
GRCh37.p13 chr 1	NC_000001.10:g.71646571_71646584del
GRCh37.p13 chr 1	NC_000001.10:g.71646572_71646584del
GRCh37.p13 chr 1	NC_000001.10:g.71646574_71646584del
GRCh37.p13 chr 1	NC_000001.10:g.71646577_71646584del
GRCh37.p13 chr 1	NC_000001.10:g.71646579_71646584del
GRCh37.p13 chr 1	NC_000001.10:g.71646581_71646584del
GRCh37.p13 chr 1	NC_000001.10:g.71646582_71646584del
GRCh37.p13 chr 1	NC_000001.10:g.71646583_71646584del
GRCh37.p13 chr 1	NC_000001.10:g.71646584del
GRCh37.p13 chr 1	NC_000001.10:g.71646584dup
GRCh37.p13 chr 1	NC_000001.10:g.71646583_71646584dup
GRCh37.p13 chr 1	NC_000001.10:g.71646582_71646584dup
GRCh37.p13 chr 1	NC_000001.10:g.71646581_71646584dup
GRCh37.p13 chr 1	NC_000001.10:g.71646580_71646584dup
GRCh37.p13 chr 1	NC_000001.10:g.71646579_71646584dup
GRCh37.p13 chr 1	NC_000001.10:g.71646578_71646584dup
GRCh37.p13 chr 1	NC_000001.10:g.71646577_71646584dup
GRCh37.p13 chr 1	NC_000001.10:g.71646576_71646584dup
GRCh37.p13 chr 1	NC_000001.10:g.71646575_71646584dup
GRCh37.p13 chr 1	NC_000001.10:g.71646574_71646584dup
GRCh37.p13 chr 1	NC_000001.10:g.71646572_71646584dup
GRCh37.p13 chr 1	NC_000001.10:g.71646584_71646585insAAAAAAAAAAAAAAAAAAAAAAAAAAAA
GRCh37.p13 chr 1	NC_000001.10:g.71646584_71646585insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA

Gene: ZRANB2-DT, ZRANB2 divergent transcript (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
ZRANB2-DT transcript	NR_046217.1: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)₂₅=	del(A)₁₄	del(A)₁₃	del(A)₁₁	del(A)₈	del(A)₆	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)₁₁	dup(A)₁₃	ins(A)₂₈	ins(A)₃₂
GRCh38.p14 chr 1	NC_000001.11:g.71180877_71180901=	NC_000001.11:g.71180888_71180901del	NC_000001.11:g.71180889_71180901del	NC_000001.11:g.71180891_71180901del	NC_000001.11:g.71180894_71180901del	NC_000001.11:g.71180896_71180901del	NC_000001.11:g.71180898_71180901del	NC_000001.11:g.71180899_71180901del	NC_000001.11:g.71180900_71180901del	NC_000001.11:g.71180901del	NC_000001.11:g.71180901dup	NC_000001.11:g.71180900_71180901dup	NC_000001.11:g.71180899_71180901dup	NC_000001.11:g.71180898_71180901dup	NC_000001.11:g.71180897_71180901dup	NC_000001.11:g.71180896_71180901dup	NC_000001.11:g.71180895_71180901dup	NC_000001.11:g.71180894_71180901dup	NC_000001.11:g.71180893_71180901dup	NC_000001.11:g.71180892_71180901dup	NC_000001.11:g.71180891_71180901dup	NC_000001.11:g.71180889_71180901dup	NC_000001.11:g.71180901_71180902insAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000001.11:g.71180901_71180902insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
GRCh37.p13 chr 1	NC_000001.10:g.71646560_71646584=	NC_000001.10:g.71646571_71646584del	NC_000001.10:g.71646572_71646584del	NC_000001.10:g.71646574_71646584del	NC_000001.10:g.71646577_71646584del	NC_000001.10:g.71646579_71646584del	NC_000001.10:g.71646581_71646584del	NC_000001.10:g.71646582_71646584del	NC_000001.10:g.71646583_71646584del	NC_000001.10:g.71646584del	NC_000001.10:g.71646584dup	NC_000001.10:g.71646583_71646584dup	NC_000001.10:g.71646582_71646584dup	NC_000001.10:g.71646581_71646584dup	NC_000001.10:g.71646580_71646584dup	NC_000001.10:g.71646579_71646584dup	NC_000001.10:g.71646578_71646584dup	NC_000001.10:g.71646577_71646584dup	NC_000001.10:g.71646576_71646584dup	NC_000001.10:g.71646575_71646584dup	NC_000001.10:g.71646574_71646584dup	NC_000001.10:g.71646572_71646584dup	NC_000001.10:g.71646584_71646585insAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000001.10:g.71646584_71646585insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA

Submissions tab displays variations originally submitted to dbSNP, now supporting this RefSNP cluster (rs). We display Submitter handle, Submission identifier, Date and Build number, when the submission appeared for the first time. Direct submissions to dbSNP have Submission ID in the form of an ss-prefixed number (ss#). Other supporting variations are listed in the table without ss#.

46 SubSNP, 33 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	HUMANGENOME_JCVI	ss95232639	Dec 05, 2013 (142)
2	PJP	ss294584903	May 09, 2011 (137)
3	SWEGEN	ss2986994400	Nov 08, 2017 (151)
4	SWEGEN	ss2986994401	Nov 08, 2017 (151)
5	SWEGEN	ss2986994402	Nov 08, 2017 (151)
6	MCHAISSO	ss3065307789	Nov 08, 2017 (151)
7	EVA	ss3826229381	Apr 25, 2020 (154)
8	GNOMAD	ss3995599432	Apr 25, 2021 (155)
9	GNOMAD	ss3995599433	Apr 25, 2021 (155)
10	GNOMAD	ss3995599434	Apr 25, 2021 (155)
11	GNOMAD	ss3995599435	Apr 25, 2021 (155)
12	GNOMAD	ss3995599436	Apr 25, 2021 (155)
13	GNOMAD	ss3995599437	Apr 25, 2021 (155)
14	GNOMAD	ss3995599438	Apr 25, 2021 (155)
15	GNOMAD	ss3995599439	Apr 25, 2021 (155)
16	GNOMAD	ss3995599440	Apr 25, 2021 (155)
17	GNOMAD	ss3995599441	Apr 25, 2021 (155)
18	GNOMAD	ss3995599442	Apr 25, 2021 (155)
19	GNOMAD	ss3995599443	Apr 25, 2021 (155)
20	GNOMAD	ss3995599444	Apr 25, 2021 (155)
21	GNOMAD	ss3995599445	Apr 25, 2021 (155)
22	GNOMAD	ss3995599447	Apr 25, 2021 (155)
23	GNOMAD	ss3995599448	Apr 25, 2021 (155)
24	GNOMAD	ss3995599449	Apr 25, 2021 (155)
25	GNOMAD	ss3995599450	Apr 25, 2021 (155)
26	GNOMAD	ss3995599451	Apr 25, 2021 (155)
27	GNOMAD	ss3995599452	Apr 25, 2021 (155)
28	GNOMAD	ss3995599453	Apr 25, 2021 (155)
29	TOPMED	ss4453706185	Apr 25, 2021 (155)
30	TOMMO_GENOMICS	ss5144448307	Apr 25, 2021 (155)
31	TOMMO_GENOMICS	ss5144448308	Apr 25, 2021 (155)
32	TOMMO_GENOMICS	ss5144448309	Apr 25, 2021 (155)
33	TOMMO_GENOMICS	ss5144448310	Apr 25, 2021 (155)
34	TOMMO_GENOMICS	ss5144448311	Apr 25, 2021 (155)
35	1000G_HIGH_COVERAGE	ss5242655534	Oct 12, 2022 (156)
36	1000G_HIGH_COVERAGE	ss5242655535	Oct 12, 2022 (156)
37	HUGCELL_USP	ss5443680815	Oct 12, 2022 (156)
38	HUGCELL_USP	ss5443680816	Oct 12, 2022 (156)
39	HUGCELL_USP	ss5443680817	Oct 12, 2022 (156)
40	TOMMO_GENOMICS	ss5669362562	Oct 12, 2022 (156)
41	TOMMO_GENOMICS	ss5669362563	Oct 12, 2022 (156)
42	TOMMO_GENOMICS	ss5669362564	Oct 12, 2022 (156)
43	TOMMO_GENOMICS	ss5669362566	Oct 12, 2022 (156)
44	TOMMO_GENOMICS	ss5669362567	Oct 12, 2022 (156)
45	EVA	ss5832109277	Oct 12, 2022 (156)
46	EVA	ss5832109278	Oct 12, 2022 (156)
47	gnomAD - Genomes Submission ignored due to conflicting rows: Row 14629556 (NC_000001.11:71180876::A 28115/45762) Row 14629557 (NC_000001.11:71180876::AA 1810/45476) Row 14629558 (NC_000001.11:71180876::AAA 329/45742)...	-	Apr 25, 2021 (155)
48	gnomAD - Genomes Submission ignored due to conflicting rows: Row 14629556 (NC_000001.11:71180876::A 28115/45762) Row 14629557 (NC_000001.11:71180876::AA 1810/45476) Row 14629558 (NC_000001.11:71180876::AAA 329/45742)...	-	Apr 25, 2021 (155)
49	gnomAD - Genomes Submission ignored due to conflicting rows: Row 14629556 (NC_000001.11:71180876::A 28115/45762) Row 14629557 (NC_000001.11:71180876::AA 1810/45476) Row 14629558 (NC_000001.11:71180876::AAA 329/45742)...	-	Apr 25, 2021 (155)
50	gnomAD - Genomes Submission ignored due to conflicting rows: Row 14629556 (NC_000001.11:71180876::A 28115/45762) Row 14629557 (NC_000001.11:71180876::AA 1810/45476) Row 14629558 (NC_000001.11:71180876::AAA 329/45742)...	-	Apr 25, 2021 (155)
51	gnomAD - Genomes Submission ignored due to conflicting rows: Row 14629556 (NC_000001.11:71180876::A 28115/45762) Row 14629557 (NC_000001.11:71180876::AA 1810/45476) Row 14629558 (NC_000001.11:71180876::AAA 329/45742)...	-	Apr 25, 2021 (155)
52	gnomAD - Genomes Submission ignored due to conflicting rows: Row 14629556 (NC_000001.11:71180876::A 28115/45762) Row 14629557 (NC_000001.11:71180876::AA 1810/45476) Row 14629558 (NC_000001.11:71180876::AAA 329/45742)...	-	Apr 25, 2021 (155)
53	gnomAD - Genomes Submission ignored due to conflicting rows: Row 14629556 (NC_000001.11:71180876::A 28115/45762) Row 14629557 (NC_000001.11:71180876::AA 1810/45476) Row 14629558 (NC_000001.11:71180876::AAA 329/45742)...	-	Apr 25, 2021 (155)
54	gnomAD - Genomes Submission ignored due to conflicting rows: Row 14629556 (NC_000001.11:71180876::A 28115/45762) Row 14629557 (NC_000001.11:71180876::AA 1810/45476) Row 14629558 (NC_000001.11:71180876::AAA 329/45742)...	-	Apr 25, 2021 (155)
55	gnomAD - Genomes Submission ignored due to conflicting rows: Row 14629556 (NC_000001.11:71180876::A 28115/45762) Row 14629557 (NC_000001.11:71180876::AA 1810/45476) Row 14629558 (NC_000001.11:71180876::AAA 329/45742)...	-	Apr 25, 2021 (155)
56	gnomAD - Genomes Submission ignored due to conflicting rows: Row 14629556 (NC_000001.11:71180876::A 28115/45762) Row 14629557 (NC_000001.11:71180876::AA 1810/45476) Row 14629558 (NC_000001.11:71180876::AAA 329/45742)...	-	Apr 25, 2021 (155)
57	gnomAD - Genomes Submission ignored due to conflicting rows: Row 14629556 (NC_000001.11:71180876::A 28115/45762) Row 14629557 (NC_000001.11:71180876::AA 1810/45476) Row 14629558 (NC_000001.11:71180876::AAA 329/45742)...	-	Apr 25, 2021 (155)
58	gnomAD - Genomes Submission ignored due to conflicting rows: Row 14629556 (NC_000001.11:71180876::A 28115/45762) Row 14629557 (NC_000001.11:71180876::AA 1810/45476) Row 14629558 (NC_000001.11:71180876::AAA 329/45742)...	-	Apr 25, 2021 (155)
59	gnomAD - Genomes Submission ignored due to conflicting rows: Row 14629556 (NC_000001.11:71180876::A 28115/45762) Row 14629557 (NC_000001.11:71180876::AA 1810/45476) Row 14629558 (NC_000001.11:71180876::AAA 329/45742)...	-	Apr 25, 2021 (155)
60	gnomAD - Genomes Submission ignored due to conflicting rows: Row 14629556 (NC_000001.11:71180876::A 28115/45762) Row 14629557 (NC_000001.11:71180876::AA 1810/45476) Row 14629558 (NC_000001.11:71180876::AAA 329/45742)...	-	Apr 25, 2021 (155)
61	gnomAD - Genomes Submission ignored due to conflicting rows: Row 14629556 (NC_000001.11:71180876::A 28115/45762) Row 14629557 (NC_000001.11:71180876::AA 1810/45476) Row 14629558 (NC_000001.11:71180876::AAA 329/45742)...	-	Apr 25, 2021 (155)
62	gnomAD - Genomes Submission ignored due to conflicting rows: Row 14629556 (NC_000001.11:71180876::A 28115/45762) Row 14629557 (NC_000001.11:71180876::AA 1810/45476) Row 14629558 (NC_000001.11:71180876::AAA 329/45742)...	-	Apr 25, 2021 (155)
63	gnomAD - Genomes Submission ignored due to conflicting rows: Row 14629556 (NC_000001.11:71180876::A 28115/45762) Row 14629557 (NC_000001.11:71180876::AA 1810/45476) Row 14629558 (NC_000001.11:71180876::AAA 329/45742)...	-	Apr 25, 2021 (155)
64	gnomAD - Genomes Submission ignored due to conflicting rows: Row 14629556 (NC_000001.11:71180876::A 28115/45762) Row 14629557 (NC_000001.11:71180876::AA 1810/45476) Row 14629558 (NC_000001.11:71180876::AAA 329/45742)...	-	Apr 25, 2021 (155)
65	gnomAD - Genomes Submission ignored due to conflicting rows: Row 14629556 (NC_000001.11:71180876::A 28115/45762) Row 14629557 (NC_000001.11:71180876::AA 1810/45476) Row 14629558 (NC_000001.11:71180876::AAA 329/45742)...	-	Apr 25, 2021 (155)
66	gnomAD - Genomes Submission ignored due to conflicting rows: Row 14629556 (NC_000001.11:71180876::A 28115/45762) Row 14629557 (NC_000001.11:71180876::AA 1810/45476) Row 14629558 (NC_000001.11:71180876::AAA 329/45742)...	-	Apr 25, 2021 (155)
67	gnomAD - Genomes Submission ignored due to conflicting rows: Row 14629556 (NC_000001.11:71180876::A 28115/45762) Row 14629557 (NC_000001.11:71180876::AA 1810/45476) Row 14629558 (NC_000001.11:71180876::AAA 329/45742)...	-	Apr 25, 2021 (155)
68	8.3KJPN Submission ignored due to conflicting rows: Row 2417614 (NC_000001.10:71646559::A 2627/16214) Row 2417615 (NC_000001.10:71646559:A: 67/16214) Row 2417616 (NC_000001.10:71646559::AA 226/16214)...	-	Apr 25, 2021 (155)
69	8.3KJPN Submission ignored due to conflicting rows: Row 2417614 (NC_000001.10:71646559::A 2627/16214) Row 2417615 (NC_000001.10:71646559:A: 67/16214) Row 2417616 (NC_000001.10:71646559::AA 226/16214)...	-	Apr 25, 2021 (155)
70	8.3KJPN Submission ignored due to conflicting rows: Row 2417614 (NC_000001.10:71646559::A 2627/16214) Row 2417615 (NC_000001.10:71646559:A: 67/16214) Row 2417616 (NC_000001.10:71646559::AA 226/16214)...	-	Apr 25, 2021 (155)
71	8.3KJPN Submission ignored due to conflicting rows: Row 2417614 (NC_000001.10:71646559::A 2627/16214) Row 2417615 (NC_000001.10:71646559:A: 67/16214) Row 2417616 (NC_000001.10:71646559::AA 226/16214)...	-	Apr 25, 2021 (155)
72	8.3KJPN Submission ignored due to conflicting rows: Row 2417614 (NC_000001.10:71646559::A 2627/16214) Row 2417615 (NC_000001.10:71646559:A: 67/16214) Row 2417616 (NC_000001.10:71646559::AA 226/16214)...	-	Apr 25, 2021 (155)
73	14KJPN Submission ignored due to conflicting rows: Row 3199666 (NC_000001.11:71180876::A 4702/27314) Row 3199667 (NC_000001.11:71180876:A: 113/27314) Row 3199668 (NC_000001.11:71180876::AA 358/27314)...	-	Oct 12, 2022 (156)
74	14KJPN Submission ignored due to conflicting rows: Row 3199666 (NC_000001.11:71180876::A 4702/27314) Row 3199667 (NC_000001.11:71180876:A: 113/27314) Row 3199668 (NC_000001.11:71180876::AA 358/27314)...	-	Oct 12, 2022 (156)
75	14KJPN Submission ignored due to conflicting rows: Row 3199666 (NC_000001.11:71180876::A 4702/27314) Row 3199667 (NC_000001.11:71180876:A: 113/27314) Row 3199668 (NC_000001.11:71180876::AA 358/27314)...	-	Oct 12, 2022 (156)
76	14KJPN Submission ignored due to conflicting rows: Row 3199666 (NC_000001.11:71180876::A 4702/27314) Row 3199667 (NC_000001.11:71180876:A: 113/27314) Row 3199668 (NC_000001.11:71180876::AA 358/27314)...	-	Oct 12, 2022 (156)
77	14KJPN Submission ignored due to conflicting rows: Row 3199666 (NC_000001.11:71180876::A 4702/27314) Row 3199667 (NC_000001.11:71180876:A: 113/27314) Row 3199668 (NC_000001.11:71180876::AA 358/27314)...	-	Oct 12, 2022 (156)
78	TopMed	NC_000001.11 - 71180877	Apr 25, 2021 (155)
79	ALFA	NC_000001.11 - 71180877	Apr 25, 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)
rs71095933	May 11, 2012 (137)
rs71694148	May 11, 2012 (137)
rs140879605	Sep 17, 2011 (135)
rs397980474	Aug 21, 2014 (142)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss3995599453	NC_000001.11:71180876:AAAAAAAAAAAA… NC_000001.11:71180876:AAAAAAAAAAAAAA:	NC_000001.11:71180876:AAAAAAAAAAAA… NC_000001.11:71180876:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA	(self)
483183130	NC_000001.11:71180876:AAAAAAAAAAAA… NC_000001.11:71180876:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA	NC_000001.11:71180876:AAAAAAAAAAAA… NC_000001.11:71180876:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA	(self)
483183130	NC_000001.11:71180876:AAAAAAAAAAAA… NC_000001.11:71180876:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	NC_000001.11:71180876:AAAAAAAAAAAA… NC_000001.11:71180876:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
483183130	NC_000001.11:71180876:AAAAAAAAAAAA… NC_000001.11:71180876:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	NC_000001.11:71180876:AAAAAAAAAAAA… NC_000001.11:71180876:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
17312520, ss3995599452, ss4453706185	NC_000001.11:71180876:AAAAAAAA:	NC_000001.11:71180876:AAAAAAAAAAAA… NC_000001.11:71180876:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
483183130	NC_000001.11:71180876:AAAAAAAAAAAA… NC_000001.11:71180876:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	NC_000001.11:71180876:AAAAAAAAAAAA… NC_000001.11:71180876:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss3995599451	NC_000001.11:71180876:AAAAAA:	NC_000001.11:71180876:AAAAAAAAAAAA… NC_000001.11:71180876:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
483183130	NC_000001.11:71180876:AAAAAAAAAAAA… NC_000001.11:71180876:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	NC_000001.11:71180876:AAAAAAAAAAAA… NC_000001.11:71180876:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss3995599450	NC_000001.11:71180876:AAAA:	NC_000001.11:71180876:AAAAAAAAAAAA… NC_000001.11:71180876:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
483183130	NC_000001.11:71180876:AAAAAAAAAAAA… NC_000001.11:71180876:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	NC_000001.11:71180876:AAAAAAAAAAAA… NC_000001.11:71180876:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
ss3995599449	NC_000001.11:71180876:AAA:	NC_000001.11:71180876:AAAAAAAAAAAA… NC_000001.11:71180876:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
483183130	NC_000001.11:71180876:AAAAAAAAAAAA… NC_000001.11:71180876:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	NC_000001.11:71180876:AAAAAAAAAAAA… NC_000001.11:71180876:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
ss3995599448	NC_000001.11:71180876:AA:	NC_000001.11:71180876:AAAAAAAAAAAA… NC_000001.11:71180876:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
483183130	NC_000001.11:71180876:AAAAAAAAAAAA… NC_000001.11:71180876:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	NC_000001.11:71180876:AAAAAAAAAAAA… NC_000001.11:71180876:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss5144448308	NC_000001.10:71646559:A:	NC_000001.11:71180876:AAAAAAAAAAAA… NC_000001.11:71180876:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3995599447, ss5242655535, ss5443680815, ss5669362563	NC_000001.11:71180876:A:	NC_000001.11:71180876:AAAAAAAAAAAA… NC_000001.11:71180876:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
483183130	NC_000001.11:71180876:AAAAAAAAAAAA… NC_000001.11:71180876:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	NC_000001.11:71180876:AAAAAAAAAAAA… NC_000001.11:71180876:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss294584903	NC_000001.9:71419172::A	NC_000001.11:71180876:AAAAAAAAAAAA… NC_000001.11:71180876:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss2986994401, ss3826229381, ss5144448307	NC_000001.10:71646559::A	NC_000001.11:71180876:AAAAAAAAAAAA… NC_000001.11:71180876:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3065307789, ss3995599432, ss5443680816, ss5669362562	NC_000001.11:71180876::A	NC_000001.11:71180876:AAAAAAAAAAAA… NC_000001.11:71180876:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
483183130	NC_000001.11:71180876:AAAAAAAAAAAA… NC_000001.11:71180876:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000001.11:71180876:AAAAAAAAAAAA… NC_000001.11:71180876:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss95232639	NT_032977.9:41618502::A	NC_000001.11:71180876:AAAAAAAAAAAA… NC_000001.11:71180876:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss2986994400, ss5144448309, ss5832109277	NC_000001.10:71646559::AA	NC_000001.11:71180876:AAAAAAAAAAAA… NC_000001.11:71180876:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3995599433, ss5443680817, ss5669362564	NC_000001.11:71180876::AA	NC_000001.11:71180876:AAAAAAAAAAAA… NC_000001.11:71180876:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
483183130	NC_000001.11:71180876:AAAAAAAAAAAA… NC_000001.11:71180876:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000001.11:71180876:AAAAAAAAAAAA… NC_000001.11:71180876:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss2986994402, ss5144448310, ss5832109278	NC_000001.10:71646559::AAA	NC_000001.11:71180876:AAAAAAAAAAAA… NC_000001.11:71180876:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3995599434, ss5242655534, ss5669362566	NC_000001.11:71180876::AAA	NC_000001.11:71180876:AAAAAAAAAAAA… NC_000001.11:71180876:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
483183130	NC_000001.11:71180876:AAAAAAAAAAAA… NC_000001.11:71180876:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000001.11:71180876:AAAAAAAAAAAA… NC_000001.11:71180876:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3995599435	NC_000001.11:71180876::AAAA	NC_000001.11:71180876:AAAAAAAAAAAA… NC_000001.11:71180876:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
483183130	NC_000001.11:71180876:AAAAAAAAAAAA… NC_000001.11:71180876:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000001.11:71180876:AAAAAAAAAAAA… NC_000001.11:71180876:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3995599436	NC_000001.11:71180876::AAAAA	NC_000001.11:71180876:AAAAAAAAAAAA… NC_000001.11:71180876:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss5144448311	NC_000001.10:71646559::AAAAAA	NC_000001.11:71180876:AAAAAAAAAAAA… NC_000001.11:71180876:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3995599437	NC_000001.11:71180876::AAAAAA	NC_000001.11:71180876:AAAAAAAAAAAA… NC_000001.11:71180876:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3995599438, ss5669362567	NC_000001.11:71180876::AAAAAAA	NC_000001.11:71180876:AAAAAAAAAAAA… NC_000001.11:71180876:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3995599439	NC_000001.11:71180876::AAAAAAAA	NC_000001.11:71180876:AAAAAAAAAAAA… NC_000001.11:71180876:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3995599440	NC_000001.11:71180876::AAAAAAAAA	NC_000001.11:71180876:AAAAAAAAAAAA… NC_000001.11:71180876:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3995599441	NC_000001.11:71180876::AAAAAAAAAA	NC_000001.11:71180876:AAAAAAAAAAAA… NC_000001.11:71180876:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3995599442	NC_000001.11:71180876::AAAAAAAAAAA	NC_000001.11:71180876:AAAAAAAAAAAA… NC_000001.11:71180876:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3995599443	NC_000001.11:71180876::AAAAAAAAAAA… NC_000001.11:71180876::AAAAAAAAAAAAA	NC_000001.11:71180876:AAAAAAAAAAAA… NC_000001.11:71180876:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3995599444	NC_000001.11:71180876::AAAAAAAAAAA… NC_000001.11:71180876::AAAAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000001.11:71180876:AAAAAAAAAAAA… NC_000001.11:71180876:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3995599445	NC_000001.11:71180876::AAAAAAAAAAA… NC_000001.11:71180876::AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000001.11:71180876:AAAAAAAAAAAA… NC_000001.11:71180876:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)

Removed from this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Destination RSIDs
ss3079557027	NC_000001.11:71180876:AAAAAAAAAAA:	NC_000001.11:71180876:AAAAAAAAAAAA… NC_000001.11:71180876:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA

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

No publications for rs11451861

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

rs11451861