Name: rs34666904
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.

rs34666904

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr11:75295222-75295246 (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)₁₂ / d…
del(A)₁₄ / del(A)₁₃ / del(A)₁₂ / del(A)₁₀ / 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
Variation Type: Indel Insertion and Deletion
Frequency: del(A)₁₄=0.000004 (1/264690, TOPMED)
del(A)₁₄=0.0000 (0/1454, ALFA)
del(A)₁₃=0.0000 (0/1454, ALFA) (+ 15 more)
del(A)₁₂=0.0000 (0/1454, ALFA)
del(A)₁₀=0.0000 (0/1454, ALFA)
del(A)₉=0.0000 (0/1454, ALFA)
del(A)₈=0.0000 (0/1454, ALFA)
del(A)₇=0.0000 (0/1454, ALFA)
del(A)₅=0.0000 (0/1454, ALFA)
del(A)₄=0.0000 (0/1454, ALFA)
delAAA=0.0000 (0/1454, ALFA)
delAA=0.0000 (0/1454, ALFA)
delA=0.0000 (0/1454, ALFA)
dupA=0.0000 (0/1454, ALFA)
dupAA=0.0000 (0/1454, ALFA)
dupAAA=0.0000 (0/1454, ALFA)
dup(A)₄=0.0000 (0/1454, ALFA)
dup(A)₅=0.0000 (0/1454, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: ARRB1 : 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	1454	AAAAAAAAAAAAAAAAAAAAAAAAA=1.0000	AAAAAAAAAAA=0.0000, AAAAAAAAAAAA=0.0000, AAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAA=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, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000	1.0	N/A
European	Sub	852	AAAAAAAAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=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, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	N/A
African	Sub	328	AAAAAAAAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=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, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	N/A
African Others	Sub	12	AAAAAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=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, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
African American	Sub	316	AAAAAAAAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=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, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	N/A
Asian	Sub	32	AAAAAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=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, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
East Asian	Sub	28	AAAAAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=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, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Other Asian	Sub	4	AAAAAAAAAAAAAAAAAAAAAAAAA=1.0	AAAAAAAAAAA=0.0, AAAAAAAAAAAA=0.0, AAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAA=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, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0	1.0	N/A
Latin American 1	Sub	14	AAAAAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=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, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Latin American 2	Sub	152	AAAAAAAAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=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, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	N/A
South Asian	Sub	10	AAAAAAAAAAAAAAAAAAAAAAAAA=1.0	AAAAAAAAAAA=0.0, AAAAAAAAAAAA=0.0, AAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAA=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, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0	1.0	N/A
Other	Sub	66	AAAAAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=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, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	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=0.999996	del(A)₁₄=0.000004
Allele Frequency Aggregator	Total	Global	1454	(A)₂₅=1.0000	del(A)₁₄=0.0000, del(A)₁₃=0.0000, del(A)₁₂=0.0000, del(A)₁₀=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, dupAAA=0.0000, dup(A)₄=0.0000, dup(A)₅=0.0000
Allele Frequency Aggregator	European	Sub	852	(A)₂₅=1.000	del(A)₁₄=0.000, del(A)₁₃=0.000, del(A)₁₂=0.000, del(A)₁₀=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, dupAAA=0.000, dup(A)₄=0.000, dup(A)₅=0.000
Allele Frequency Aggregator	African	Sub	328	(A)₂₅=1.000	del(A)₁₄=0.000, del(A)₁₃=0.000, del(A)₁₂=0.000, del(A)₁₀=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, dupAAA=0.000, dup(A)₄=0.000, dup(A)₅=0.000
Allele Frequency Aggregator	Latin American 2	Sub	152	(A)₂₅=1.000	del(A)₁₄=0.000, del(A)₁₃=0.000, del(A)₁₂=0.000, del(A)₁₀=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, dupAAA=0.000, dup(A)₄=0.000, dup(A)₅=0.000
Allele Frequency Aggregator	Other	Sub	66	(A)₂₅=1.00	del(A)₁₄=0.00, del(A)₁₃=0.00, del(A)₁₂=0.00, del(A)₁₀=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, dupAAA=0.00, dup(A)₄=0.00, dup(A)₅=0.00
Allele Frequency Aggregator	Asian	Sub	32	(A)₂₅=1.00	del(A)₁₄=0.00, del(A)₁₃=0.00, del(A)₁₂=0.00, del(A)₁₀=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, dupAAA=0.00, dup(A)₄=0.00, dup(A)₅=0.00
Allele Frequency Aggregator	Latin American 1	Sub	14	(A)₂₅=1.00	del(A)₁₄=0.00, del(A)₁₃=0.00, del(A)₁₂=0.00, del(A)₁₀=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, dupAAA=0.00, dup(A)₄=0.00, dup(A)₅=0.00
Allele Frequency Aggregator	South Asian	Sub	10	(A)₂₅=1.0	del(A)₁₄=0.0, del(A)₁₃=0.0, del(A)₁₂=0.0, del(A)₁₀=0.0, del(A)₉=0.0, del(A)₈=0.0, del(A)₇=0.0, del(A)₅=0.0, del(A)₄=0.0, delAAA=0.0, delAA=0.0, delA=0.0, dupA=0.0, dupAA=0.0, dupAAA=0.0, dup(A)₄=0.0, dup(A)₅=0.0

Variant Details tab shows known variant placements on genomic sequences: chromosomes (NC_), RefSeqGene, pseudogenes or genomic regions (NG_), and in a separate table: on transcripts (NM_) and protein sequences (NP_). The corresponding transcript and protein locations are listed in adjacent lines, along with molecular consequences from Sequence Ontology. When no protein placement is available, only the transcript is listed. Column "Codon[Amino acid]" shows the actual base change in the format of "Reference > Alternate" allele, including the nucleotide codon change in transcripts, and the amino acid change in proteins, respectively, allowing for known ribosomal slippage sites. To view nucleotides adjacent to the variant use the Genomic View at the bottom of the page - zoom into the sequence until the nucleotides around the variant become visible.

Genomic Placements

Sequence name	Change
GRCh38.p14 chr 11	NC_000011.10:g.75295233_75295246del
GRCh38.p14 chr 11	NC_000011.10:g.75295234_75295246del
GRCh38.p14 chr 11	NC_000011.10:g.75295235_75295246del
GRCh38.p14 chr 11	NC_000011.10:g.75295237_75295246del
GRCh38.p14 chr 11	NC_000011.10:g.75295238_75295246del
GRCh38.p14 chr 11	NC_000011.10:g.75295239_75295246del
GRCh38.p14 chr 11	NC_000011.10:g.75295240_75295246del
GRCh38.p14 chr 11	NC_000011.10:g.75295242_75295246del
GRCh38.p14 chr 11	NC_000011.10:g.75295243_75295246del
GRCh38.p14 chr 11	NC_000011.10:g.75295244_75295246del
GRCh38.p14 chr 11	NC_000011.10:g.75295245_75295246del
GRCh38.p14 chr 11	NC_000011.10:g.75295246del
GRCh38.p14 chr 11	NC_000011.10:g.75295246dup
GRCh38.p14 chr 11	NC_000011.10:g.75295245_75295246dup
GRCh38.p14 chr 11	NC_000011.10:g.75295244_75295246dup
GRCh38.p14 chr 11	NC_000011.10:g.75295243_75295246dup
GRCh38.p14 chr 11	NC_000011.10:g.75295242_75295246dup
GRCh38.p14 chr 11	NC_000011.10:g.75295241_75295246dup
GRCh38.p14 chr 11	NC_000011.10:g.75295240_75295246dup
GRCh37.p13 chr 11	NC_000011.9:g.75006277_75006290del
GRCh37.p13 chr 11	NC_000011.9:g.75006278_75006290del
GRCh37.p13 chr 11	NC_000011.9:g.75006279_75006290del
GRCh37.p13 chr 11	NC_000011.9:g.75006281_75006290del
GRCh37.p13 chr 11	NC_000011.9:g.75006282_75006290del
GRCh37.p13 chr 11	NC_000011.9:g.75006283_75006290del
GRCh37.p13 chr 11	NC_000011.9:g.75006284_75006290del
GRCh37.p13 chr 11	NC_000011.9:g.75006286_75006290del
GRCh37.p13 chr 11	NC_000011.9:g.75006287_75006290del
GRCh37.p13 chr 11	NC_000011.9:g.75006288_75006290del
GRCh37.p13 chr 11	NC_000011.9:g.75006289_75006290del
GRCh37.p13 chr 11	NC_000011.9:g.75006290del
GRCh37.p13 chr 11	NC_000011.9:g.75006290dup
GRCh37.p13 chr 11	NC_000011.9:g.75006289_75006290dup
GRCh37.p13 chr 11	NC_000011.9:g.75006288_75006290dup
GRCh37.p13 chr 11	NC_000011.9:g.75006287_75006290dup
GRCh37.p13 chr 11	NC_000011.9:g.75006286_75006290dup
GRCh37.p13 chr 11	NC_000011.9:g.75006285_75006290dup
GRCh37.p13 chr 11	NC_000011.9:g.75006284_75006290dup
ARRB1 RefSeqGene	NG_028118.1:g.61597_61610del
ARRB1 RefSeqGene	NG_028118.1:g.61598_61610del
ARRB1 RefSeqGene	NG_028118.1:g.61599_61610del
ARRB1 RefSeqGene	NG_028118.1:g.61601_61610del
ARRB1 RefSeqGene	NG_028118.1:g.61602_61610del
ARRB1 RefSeqGene	NG_028118.1:g.61603_61610del
ARRB1 RefSeqGene	NG_028118.1:g.61604_61610del
ARRB1 RefSeqGene	NG_028118.1:g.61606_61610del
ARRB1 RefSeqGene	NG_028118.1:g.61607_61610del
ARRB1 RefSeqGene	NG_028118.1:g.61608_61610del
ARRB1 RefSeqGene	NG_028118.1:g.61609_61610del
ARRB1 RefSeqGene	NG_028118.1:g.61610del
ARRB1 RefSeqGene	NG_028118.1:g.61610dup
ARRB1 RefSeqGene	NG_028118.1:g.61609_61610dup
ARRB1 RefSeqGene	NG_028118.1:g.61608_61610dup
ARRB1 RefSeqGene	NG_028118.1:g.61607_61610dup
ARRB1 RefSeqGene	NG_028118.1:g.61606_61610dup
ARRB1 RefSeqGene	NG_028118.1:g.61605_61610dup
ARRB1 RefSeqGene	NG_028118.1:g.61604_61610dup

Gene: ARRB1, arrestin beta 1 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
ARRB1 transcript variant 1	NM_004041.5:c.21-5196_21-… NM_004041.5:c.21-5196_21-5183del	N/A	Intron Variant
ARRB1 transcript variant 2	NM_020251.4:c.21-5196_21-… NM_020251.4:c.21-5196_21-5183del	N/A	Intron Variant
ARRB1 transcript variant X3	XM_011545034.2:c.114-5196… XM_011545034.2:c.114-5196_114-5183del	N/A	Intron Variant
ARRB1 transcript variant X5	XM_011545035.2:c.114-5196… XM_011545035.2:c.114-5196_114-5183del	N/A	Intron Variant
ARRB1 transcript variant X1	XM_017017750.1:c.114-5196… XM_017017750.1:c.114-5196_114-5183del	N/A	Intron Variant
ARRB1 transcript variant X2	XM_017017751.1:c.114-5196… XM_017017751.1:c.114-5196_114-5183del	N/A	Intron Variant
ARRB1 transcript variant X4	XM_017017752.3:c.21-5196_… XM_017017752.3:c.21-5196_21-5183del	N/A	Intron Variant
ARRB1 transcript variant X6	XM_017017753.1:c.6-5196_6… XM_017017753.1:c.6-5196_6-5183del	N/A	Intron Variant
ARRB1 transcript variant X7	XM_017017754.3:c.21-5196_… XM_017017754.3:c.21-5196_21-5183del	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)₁₂	del(A)₁₀	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
GRCh38.p14 chr 11	NC_000011.10:g.75295222_75295246=	NC_000011.10:g.75295233_75295246del	NC_000011.10:g.75295234_75295246del	NC_000011.10:g.75295235_75295246del	NC_000011.10:g.75295237_75295246del	NC_000011.10:g.75295238_75295246del	NC_000011.10:g.75295239_75295246del	NC_000011.10:g.75295240_75295246del	NC_000011.10:g.75295242_75295246del	NC_000011.10:g.75295243_75295246del	NC_000011.10:g.75295244_75295246del	NC_000011.10:g.75295245_75295246del	NC_000011.10:g.75295246del	NC_000011.10:g.75295246dup	NC_000011.10:g.75295245_75295246dup	NC_000011.10:g.75295244_75295246dup	NC_000011.10:g.75295243_75295246dup	NC_000011.10:g.75295242_75295246dup	NC_000011.10:g.75295241_75295246dup	NC_000011.10:g.75295240_75295246dup
GRCh37.p13 chr 11	NC_000011.9:g.75006266_75006290=	NC_000011.9:g.75006277_75006290del	NC_000011.9:g.75006278_75006290del	NC_000011.9:g.75006279_75006290del	NC_000011.9:g.75006281_75006290del	NC_000011.9:g.75006282_75006290del	NC_000011.9:g.75006283_75006290del	NC_000011.9:g.75006284_75006290del	NC_000011.9:g.75006286_75006290del	NC_000011.9:g.75006287_75006290del	NC_000011.9:g.75006288_75006290del	NC_000011.9:g.75006289_75006290del	NC_000011.9:g.75006290del	NC_000011.9:g.75006290dup	NC_000011.9:g.75006289_75006290dup	NC_000011.9:g.75006288_75006290dup	NC_000011.9:g.75006287_75006290dup	NC_000011.9:g.75006286_75006290dup	NC_000011.9:g.75006285_75006290dup	NC_000011.9:g.75006284_75006290dup
ARRB1 RefSeqGene	NG_028118.1:g.61586_61610=	NG_028118.1:g.61597_61610del	NG_028118.1:g.61598_61610del	NG_028118.1:g.61599_61610del	NG_028118.1:g.61601_61610del	NG_028118.1:g.61602_61610del	NG_028118.1:g.61603_61610del	NG_028118.1:g.61604_61610del	NG_028118.1:g.61606_61610del	NG_028118.1:g.61607_61610del	NG_028118.1:g.61608_61610del	NG_028118.1:g.61609_61610del	NG_028118.1:g.61610del	NG_028118.1:g.61610dup	NG_028118.1:g.61609_61610dup	NG_028118.1:g.61608_61610dup	NG_028118.1:g.61607_61610dup	NG_028118.1:g.61606_61610dup	NG_028118.1:g.61605_61610dup	NG_028118.1:g.61604_61610dup
ARRB1 transcript variant 1	NM_004041.4:c.21-5183=	NM_004041.4:c.21-5196_21-5183del	NM_004041.4:c.21-5195_21-5183del	NM_004041.4:c.21-5194_21-5183del	NM_004041.4:c.21-5192_21-5183del	NM_004041.4:c.21-5191_21-5183del	NM_004041.4:c.21-5190_21-5183del	NM_004041.4:c.21-5189_21-5183del	NM_004041.4:c.21-5187_21-5183del	NM_004041.4:c.21-5186_21-5183del	NM_004041.4:c.21-5185_21-5183del	NM_004041.4:c.21-5184_21-5183del	NM_004041.4:c.21-5183del	NM_004041.4:c.21-5183dup	NM_004041.4:c.21-5184_21-5183dup	NM_004041.4:c.21-5185_21-5183dup	NM_004041.4:c.21-5186_21-5183dup	NM_004041.4:c.21-5187_21-5183dup	NM_004041.4:c.21-5188_21-5183dup	NM_004041.4:c.21-5189_21-5183dup
ARRB1 transcript variant 1	NM_004041.5:c.21-5183=	NM_004041.5:c.21-5196_21-5183del	NM_004041.5:c.21-5195_21-5183del	NM_004041.5:c.21-5194_21-5183del	NM_004041.5:c.21-5192_21-5183del	NM_004041.5:c.21-5191_21-5183del	NM_004041.5:c.21-5190_21-5183del	NM_004041.5:c.21-5189_21-5183del	NM_004041.5:c.21-5187_21-5183del	NM_004041.5:c.21-5186_21-5183del	NM_004041.5:c.21-5185_21-5183del	NM_004041.5:c.21-5184_21-5183del	NM_004041.5:c.21-5183del	NM_004041.5:c.21-5183dup	NM_004041.5:c.21-5184_21-5183dup	NM_004041.5:c.21-5185_21-5183dup	NM_004041.5:c.21-5186_21-5183dup	NM_004041.5:c.21-5187_21-5183dup	NM_004041.5:c.21-5188_21-5183dup	NM_004041.5:c.21-5189_21-5183dup
ARRB1 transcript variant 2	NM_020251.3:c.21-5183=	NM_020251.3:c.21-5196_21-5183del	NM_020251.3:c.21-5195_21-5183del	NM_020251.3:c.21-5194_21-5183del	NM_020251.3:c.21-5192_21-5183del	NM_020251.3:c.21-5191_21-5183del	NM_020251.3:c.21-5190_21-5183del	NM_020251.3:c.21-5189_21-5183del	NM_020251.3:c.21-5187_21-5183del	NM_020251.3:c.21-5186_21-5183del	NM_020251.3:c.21-5185_21-5183del	NM_020251.3:c.21-5184_21-5183del	NM_020251.3:c.21-5183del	NM_020251.3:c.21-5183dup	NM_020251.3:c.21-5184_21-5183dup	NM_020251.3:c.21-5185_21-5183dup	NM_020251.3:c.21-5186_21-5183dup	NM_020251.3:c.21-5187_21-5183dup	NM_020251.3:c.21-5188_21-5183dup	NM_020251.3:c.21-5189_21-5183dup
ARRB1 transcript variant 2	NM_020251.4:c.21-5183=	NM_020251.4:c.21-5196_21-5183del	NM_020251.4:c.21-5195_21-5183del	NM_020251.4:c.21-5194_21-5183del	NM_020251.4:c.21-5192_21-5183del	NM_020251.4:c.21-5191_21-5183del	NM_020251.4:c.21-5190_21-5183del	NM_020251.4:c.21-5189_21-5183del	NM_020251.4:c.21-5187_21-5183del	NM_020251.4:c.21-5186_21-5183del	NM_020251.4:c.21-5185_21-5183del	NM_020251.4:c.21-5184_21-5183del	NM_020251.4:c.21-5183del	NM_020251.4:c.21-5183dup	NM_020251.4:c.21-5184_21-5183dup	NM_020251.4:c.21-5185_21-5183dup	NM_020251.4:c.21-5186_21-5183dup	NM_020251.4:c.21-5187_21-5183dup	NM_020251.4:c.21-5188_21-5183dup	NM_020251.4:c.21-5189_21-5183dup
ARRB1 transcript variant X3	XM_005273997.1:c.33-5183=	XM_005273997.1:c.33-5196_33-5183del	XM_005273997.1:c.33-5195_33-5183del	XM_005273997.1:c.33-5194_33-5183del	XM_005273997.1:c.33-5192_33-5183del	XM_005273997.1:c.33-5191_33-5183del	XM_005273997.1:c.33-5190_33-5183del	XM_005273997.1:c.33-5189_33-5183del	XM_005273997.1:c.33-5187_33-5183del	XM_005273997.1:c.33-5186_33-5183del	XM_005273997.1:c.33-5185_33-5183del	XM_005273997.1:c.33-5184_33-5183del	XM_005273997.1:c.33-5183del	XM_005273997.1:c.33-5183dup	XM_005273997.1:c.33-5184_33-5183dup	XM_005273997.1:c.33-5185_33-5183dup	XM_005273997.1:c.33-5186_33-5183dup	XM_005273997.1:c.33-5187_33-5183dup	XM_005273997.1:c.33-5188_33-5183dup	XM_005273997.1:c.33-5189_33-5183dup
ARRB1 transcript variant X2	XM_005273998.1:c.33-5183=	XM_005273998.1:c.33-5196_33-5183del	XM_005273998.1:c.33-5195_33-5183del	XM_005273998.1:c.33-5194_33-5183del	XM_005273998.1:c.33-5192_33-5183del	XM_005273998.1:c.33-5191_33-5183del	XM_005273998.1:c.33-5190_33-5183del	XM_005273998.1:c.33-5189_33-5183del	XM_005273998.1:c.33-5187_33-5183del	XM_005273998.1:c.33-5186_33-5183del	XM_005273998.1:c.33-5185_33-5183del	XM_005273998.1:c.33-5184_33-5183del	XM_005273998.1:c.33-5183del	XM_005273998.1:c.33-5183dup	XM_005273998.1:c.33-5184_33-5183dup	XM_005273998.1:c.33-5185_33-5183dup	XM_005273998.1:c.33-5186_33-5183dup	XM_005273998.1:c.33-5187_33-5183dup	XM_005273998.1:c.33-5188_33-5183dup	XM_005273998.1:c.33-5189_33-5183dup
ARRB1 transcript variant X3	XM_005273999.1:c.6-5183=	XM_005273999.1:c.6-5196_6-5183del	XM_005273999.1:c.6-5195_6-5183del	XM_005273999.1:c.6-5194_6-5183del	XM_005273999.1:c.6-5192_6-5183del	XM_005273999.1:c.6-5191_6-5183del	XM_005273999.1:c.6-5190_6-5183del	XM_005273999.1:c.6-5189_6-5183del	XM_005273999.1:c.6-5187_6-5183del	XM_005273999.1:c.6-5186_6-5183del	XM_005273999.1:c.6-5185_6-5183del	XM_005273999.1:c.6-5184_6-5183del	XM_005273999.1:c.6-5183del	XM_005273999.1:c.6-5183dup	XM_005273999.1:c.6-5184_6-5183dup	XM_005273999.1:c.6-5185_6-5183dup	XM_005273999.1:c.6-5186_6-5183dup	XM_005273999.1:c.6-5187_6-5183dup	XM_005273999.1:c.6-5188_6-5183dup	XM_005273999.1:c.6-5189_6-5183dup
ARRB1 transcript variant X3	XM_011545034.2:c.114-5183=	XM_011545034.2:c.114-5196_114-5183del	XM_011545034.2:c.114-5195_114-5183del	XM_011545034.2:c.114-5194_114-5183del	XM_011545034.2:c.114-5192_114-5183del	XM_011545034.2:c.114-5191_114-5183del	XM_011545034.2:c.114-5190_114-5183del	XM_011545034.2:c.114-5189_114-5183del	XM_011545034.2:c.114-5187_114-5183del	XM_011545034.2:c.114-5186_114-5183del	XM_011545034.2:c.114-5185_114-5183del	XM_011545034.2:c.114-5184_114-5183del	XM_011545034.2:c.114-5183del	XM_011545034.2:c.114-5183dup	XM_011545034.2:c.114-5184_114-5183dup	XM_011545034.2:c.114-5185_114-5183dup	XM_011545034.2:c.114-5186_114-5183dup	XM_011545034.2:c.114-5187_114-5183dup	XM_011545034.2:c.114-5188_114-5183dup	XM_011545034.2:c.114-5189_114-5183dup
ARRB1 transcript variant X5	XM_011545035.2:c.114-5183=	XM_011545035.2:c.114-5196_114-5183del	XM_011545035.2:c.114-5195_114-5183del	XM_011545035.2:c.114-5194_114-5183del	XM_011545035.2:c.114-5192_114-5183del	XM_011545035.2:c.114-5191_114-5183del	XM_011545035.2:c.114-5190_114-5183del	XM_011545035.2:c.114-5189_114-5183del	XM_011545035.2:c.114-5187_114-5183del	XM_011545035.2:c.114-5186_114-5183del	XM_011545035.2:c.114-5185_114-5183del	XM_011545035.2:c.114-5184_114-5183del	XM_011545035.2:c.114-5183del	XM_011545035.2:c.114-5183dup	XM_011545035.2:c.114-5184_114-5183dup	XM_011545035.2:c.114-5185_114-5183dup	XM_011545035.2:c.114-5186_114-5183dup	XM_011545035.2:c.114-5187_114-5183dup	XM_011545035.2:c.114-5188_114-5183dup	XM_011545035.2:c.114-5189_114-5183dup
ARRB1 transcript variant X1	XM_017017750.1:c.114-5183=	XM_017017750.1:c.114-5196_114-5183del	XM_017017750.1:c.114-5195_114-5183del	XM_017017750.1:c.114-5194_114-5183del	XM_017017750.1:c.114-5192_114-5183del	XM_017017750.1:c.114-5191_114-5183del	XM_017017750.1:c.114-5190_114-5183del	XM_017017750.1:c.114-5189_114-5183del	XM_017017750.1:c.114-5187_114-5183del	XM_017017750.1:c.114-5186_114-5183del	XM_017017750.1:c.114-5185_114-5183del	XM_017017750.1:c.114-5184_114-5183del	XM_017017750.1:c.114-5183del	XM_017017750.1:c.114-5183dup	XM_017017750.1:c.114-5184_114-5183dup	XM_017017750.1:c.114-5185_114-5183dup	XM_017017750.1:c.114-5186_114-5183dup	XM_017017750.1:c.114-5187_114-5183dup	XM_017017750.1:c.114-5188_114-5183dup	XM_017017750.1:c.114-5189_114-5183dup
ARRB1 transcript variant X2	XM_017017751.1:c.114-5183=	XM_017017751.1:c.114-5196_114-5183del	XM_017017751.1:c.114-5195_114-5183del	XM_017017751.1:c.114-5194_114-5183del	XM_017017751.1:c.114-5192_114-5183del	XM_017017751.1:c.114-5191_114-5183del	XM_017017751.1:c.114-5190_114-5183del	XM_017017751.1:c.114-5189_114-5183del	XM_017017751.1:c.114-5187_114-5183del	XM_017017751.1:c.114-5186_114-5183del	XM_017017751.1:c.114-5185_114-5183del	XM_017017751.1:c.114-5184_114-5183del	XM_017017751.1:c.114-5183del	XM_017017751.1:c.114-5183dup	XM_017017751.1:c.114-5184_114-5183dup	XM_017017751.1:c.114-5185_114-5183dup	XM_017017751.1:c.114-5186_114-5183dup	XM_017017751.1:c.114-5187_114-5183dup	XM_017017751.1:c.114-5188_114-5183dup	XM_017017751.1:c.114-5189_114-5183dup
ARRB1 transcript variant X4	XM_017017752.3:c.21-5183=	XM_017017752.3:c.21-5196_21-5183del	XM_017017752.3:c.21-5195_21-5183del	XM_017017752.3:c.21-5194_21-5183del	XM_017017752.3:c.21-5192_21-5183del	XM_017017752.3:c.21-5191_21-5183del	XM_017017752.3:c.21-5190_21-5183del	XM_017017752.3:c.21-5189_21-5183del	XM_017017752.3:c.21-5187_21-5183del	XM_017017752.3:c.21-5186_21-5183del	XM_017017752.3:c.21-5185_21-5183del	XM_017017752.3:c.21-5184_21-5183del	XM_017017752.3:c.21-5183del	XM_017017752.3:c.21-5183dup	XM_017017752.3:c.21-5184_21-5183dup	XM_017017752.3:c.21-5185_21-5183dup	XM_017017752.3:c.21-5186_21-5183dup	XM_017017752.3:c.21-5187_21-5183dup	XM_017017752.3:c.21-5188_21-5183dup	XM_017017752.3:c.21-5189_21-5183dup
ARRB1 transcript variant X6	XM_017017753.1:c.6-5183=	XM_017017753.1:c.6-5196_6-5183del	XM_017017753.1:c.6-5195_6-5183del	XM_017017753.1:c.6-5194_6-5183del	XM_017017753.1:c.6-5192_6-5183del	XM_017017753.1:c.6-5191_6-5183del	XM_017017753.1:c.6-5190_6-5183del	XM_017017753.1:c.6-5189_6-5183del	XM_017017753.1:c.6-5187_6-5183del	XM_017017753.1:c.6-5186_6-5183del	XM_017017753.1:c.6-5185_6-5183del	XM_017017753.1:c.6-5184_6-5183del	XM_017017753.1:c.6-5183del	XM_017017753.1:c.6-5183dup	XM_017017753.1:c.6-5184_6-5183dup	XM_017017753.1:c.6-5185_6-5183dup	XM_017017753.1:c.6-5186_6-5183dup	XM_017017753.1:c.6-5187_6-5183dup	XM_017017753.1:c.6-5188_6-5183dup	XM_017017753.1:c.6-5189_6-5183dup
ARRB1 transcript variant X7	XM_017017754.3:c.21-5183=	XM_017017754.3:c.21-5196_21-5183del	XM_017017754.3:c.21-5195_21-5183del	XM_017017754.3:c.21-5194_21-5183del	XM_017017754.3:c.21-5192_21-5183del	XM_017017754.3:c.21-5191_21-5183del	XM_017017754.3:c.21-5190_21-5183del	XM_017017754.3:c.21-5189_21-5183del	XM_017017754.3:c.21-5187_21-5183del	XM_017017754.3:c.21-5186_21-5183del	XM_017017754.3:c.21-5185_21-5183del	XM_017017754.3:c.21-5184_21-5183del	XM_017017754.3:c.21-5183del	XM_017017754.3:c.21-5183dup	XM_017017754.3:c.21-5184_21-5183dup	XM_017017754.3:c.21-5185_21-5183dup	XM_017017754.3:c.21-5186_21-5183dup	XM_017017754.3:c.21-5187_21-5183dup	XM_017017754.3:c.21-5188_21-5183dup	XM_017017754.3:c.21-5189_21-5183dup

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#.

47 SubSNP, 25 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	ABI	ss39935628	Mar 15, 2006 (126)
2	ABI	ss39986051	Mar 14, 2006 (126)
3	HGSV	ss83156037	Dec 15, 2007 (129)
4	HUMANGENOME_JCVI	ss95573107	Dec 05, 2013 (142)
5	PJP	ss294710209	May 09, 2011 (134)
6	PJP	ss294710210	May 09, 2011 (135)
7	SWEGEN	ss3008358843	Nov 08, 2017 (151)
8	MCHAISSO	ss3063697944	Nov 17, 2017 (151)
9	MCHAISSO	ss3064523294	Nov 17, 2017 (151)
10	EVA_DECODE	ss3692097414	Jul 13, 2019 (153)
11	EVA_DECODE	ss3692097415	Jul 13, 2019 (153)
12	EVA_DECODE	ss3692097416	Jul 13, 2019 (153)
13	EVA_DECODE	ss3692097417	Jul 13, 2019 (153)
14	EVA_DECODE	ss3692097418	Jul 13, 2019 (153)
15	EVA	ss3832704157	Apr 26, 2020 (154)
16	GNOMAD	ss4237952453	Apr 26, 2021 (155)
17	GNOMAD	ss4237952454	Apr 26, 2021 (155)
18	GNOMAD	ss4237952455	Apr 26, 2021 (155)
19	GNOMAD	ss4237952456	Apr 26, 2021 (155)
20	GNOMAD	ss4237952457	Apr 26, 2021 (155)
21	GNOMAD	ss4237952458	Apr 26, 2021 (155)
22	GNOMAD	ss4237952459	Apr 26, 2021 (155)
23	GNOMAD	ss4237952460	Apr 26, 2021 (155)
24	GNOMAD	ss4237952461	Apr 26, 2021 (155)
25	GNOMAD	ss4237952462	Apr 26, 2021 (155)
26	GNOMAD	ss4237952463	Apr 26, 2021 (155)
27	GNOMAD	ss4237952464	Apr 26, 2021 (155)
28	GNOMAD	ss4237952465	Apr 26, 2021 (155)
29	GNOMAD	ss4237952466	Apr 26, 2021 (155)
30	GNOMAD	ss4237952467	Apr 26, 2021 (155)
31	TOPMED	ss4890810500	Apr 26, 2021 (155)
32	TOMMO_GENOMICS	ss5202725587	Apr 26, 2021 (155)
33	TOMMO_GENOMICS	ss5202725588	Apr 26, 2021 (155)
34	TOMMO_GENOMICS	ss5202725589	Apr 26, 2021 (155)
35	TOMMO_GENOMICS	ss5202725590	Apr 26, 2021 (155)
36	1000G_HIGH_COVERAGE	ss5287989857	Oct 16, 2022 (156)
37	1000G_HIGH_COVERAGE	ss5287989858	Oct 16, 2022 (156)
38	1000G_HIGH_COVERAGE	ss5287989859	Oct 16, 2022 (156)
39	1000G_HIGH_COVERAGE	ss5287989860	Oct 16, 2022 (156)
40	1000G_HIGH_COVERAGE	ss5287989861	Oct 16, 2022 (156)
41	HUGCELL_USP	ss5483088975	Oct 16, 2022 (156)
42	HUGCELL_USP	ss5483088976	Oct 16, 2022 (156)
43	HUGCELL_USP	ss5483088977	Oct 16, 2022 (156)
44	TOMMO_GENOMICS	ss5750844498	Oct 16, 2022 (156)
45	TOMMO_GENOMICS	ss5750844499	Oct 16, 2022 (156)
46	TOMMO_GENOMICS	ss5750844500	Oct 16, 2022 (156)
47	TOMMO_GENOMICS	ss5750844502	Oct 16, 2022 (156)
48	gnomAD - Genomes Submission ignored due to conflicting rows: Row 384405829 (NC_000011.10:75295221::A 5678/68194) Row 384405830 (NC_000011.10:75295221::AA 787/68108) Row 384405831 (NC_000011.10:75295221::AAA 94/68286)...	-	Apr 26, 2021 (155)
49	gnomAD - Genomes Submission ignored due to conflicting rows: Row 384405829 (NC_000011.10:75295221::A 5678/68194) Row 384405830 (NC_000011.10:75295221::AA 787/68108) Row 384405831 (NC_000011.10:75295221::AAA 94/68286)...	-	Apr 26, 2021 (155)
50	gnomAD - Genomes Submission ignored due to conflicting rows: Row 384405829 (NC_000011.10:75295221::A 5678/68194) Row 384405830 (NC_000011.10:75295221::AA 787/68108) Row 384405831 (NC_000011.10:75295221::AAA 94/68286)...	-	Apr 26, 2021 (155)
51	gnomAD - Genomes Submission ignored due to conflicting rows: Row 384405829 (NC_000011.10:75295221::A 5678/68194) Row 384405830 (NC_000011.10:75295221::AA 787/68108) Row 384405831 (NC_000011.10:75295221::AAA 94/68286)...	-	Apr 26, 2021 (155)
52	gnomAD - Genomes Submission ignored due to conflicting rows: Row 384405829 (NC_000011.10:75295221::A 5678/68194) Row 384405830 (NC_000011.10:75295221::AA 787/68108) Row 384405831 (NC_000011.10:75295221::AAA 94/68286)...	-	Apr 26, 2021 (155)
53	gnomAD - Genomes Submission ignored due to conflicting rows: Row 384405829 (NC_000011.10:75295221::A 5678/68194) Row 384405830 (NC_000011.10:75295221::AA 787/68108) Row 384405831 (NC_000011.10:75295221::AAA 94/68286)...	-	Apr 26, 2021 (155)
54	gnomAD - Genomes Submission ignored due to conflicting rows: Row 384405829 (NC_000011.10:75295221::A 5678/68194) Row 384405830 (NC_000011.10:75295221::AA 787/68108) Row 384405831 (NC_000011.10:75295221::AAA 94/68286)...	-	Apr 26, 2021 (155)
55	gnomAD - Genomes Submission ignored due to conflicting rows: Row 384405829 (NC_000011.10:75295221::A 5678/68194) Row 384405830 (NC_000011.10:75295221::AA 787/68108) Row 384405831 (NC_000011.10:75295221::AAA 94/68286)...	-	Apr 26, 2021 (155)
56	gnomAD - Genomes Submission ignored due to conflicting rows: Row 384405829 (NC_000011.10:75295221::A 5678/68194) Row 384405830 (NC_000011.10:75295221::AA 787/68108) Row 384405831 (NC_000011.10:75295221::AAA 94/68286)...	-	Apr 26, 2021 (155)
57	gnomAD - Genomes Submission ignored due to conflicting rows: Row 384405829 (NC_000011.10:75295221::A 5678/68194) Row 384405830 (NC_000011.10:75295221::AA 787/68108) Row 384405831 (NC_000011.10:75295221::AAA 94/68286)...	-	Apr 26, 2021 (155)
58	gnomAD - Genomes Submission ignored due to conflicting rows: Row 384405829 (NC_000011.10:75295221::A 5678/68194) Row 384405830 (NC_000011.10:75295221::AA 787/68108) Row 384405831 (NC_000011.10:75295221::AAA 94/68286)...	-	Apr 26, 2021 (155)
59	gnomAD - Genomes Submission ignored due to conflicting rows: Row 384405829 (NC_000011.10:75295221::A 5678/68194) Row 384405830 (NC_000011.10:75295221::AA 787/68108) Row 384405831 (NC_000011.10:75295221::AAA 94/68286)...	-	Apr 26, 2021 (155)
60	gnomAD - Genomes Submission ignored due to conflicting rows: Row 384405829 (NC_000011.10:75295221::A 5678/68194) Row 384405830 (NC_000011.10:75295221::AA 787/68108) Row 384405831 (NC_000011.10:75295221::AAA 94/68286)...	-	Apr 26, 2021 (155)
61	gnomAD - Genomes Submission ignored due to conflicting rows: Row 384405829 (NC_000011.10:75295221::A 5678/68194) Row 384405830 (NC_000011.10:75295221::AA 787/68108) Row 384405831 (NC_000011.10:75295221::AAA 94/68286)...	-	Apr 26, 2021 (155)
62	gnomAD - Genomes Submission ignored due to conflicting rows: Row 384405829 (NC_000011.10:75295221::A 5678/68194) Row 384405830 (NC_000011.10:75295221::AA 787/68108) Row 384405831 (NC_000011.10:75295221::AAA 94/68286)...	-	Apr 26, 2021 (155)
63	8.3KJPN Submission ignored due to conflicting rows: Row 60694894 (NC_000011.9:75006265:AA: 4122/16562) Row 60694895 (NC_000011.9:75006265:A: 1692/16562) Row 60694896 (NC_000011.9:75006265:AAA: 13/16562)...	-	Apr 26, 2021 (155)
64	8.3KJPN Submission ignored due to conflicting rows: Row 60694894 (NC_000011.9:75006265:AA: 4122/16562) Row 60694895 (NC_000011.9:75006265:A: 1692/16562) Row 60694896 (NC_000011.9:75006265:AAA: 13/16562)...	-	Apr 26, 2021 (155)
65	8.3KJPN Submission ignored due to conflicting rows: Row 60694894 (NC_000011.9:75006265:AA: 4122/16562) Row 60694895 (NC_000011.9:75006265:A: 1692/16562) Row 60694896 (NC_000011.9:75006265:AAA: 13/16562)...	-	Apr 26, 2021 (155)
66	8.3KJPN Submission ignored due to conflicting rows: Row 60694894 (NC_000011.9:75006265:AA: 4122/16562) Row 60694895 (NC_000011.9:75006265:A: 1692/16562) Row 60694896 (NC_000011.9:75006265:AAA: 13/16562)...	-	Apr 26, 2021 (155)
67	14KJPN Submission ignored due to conflicting rows: Row 84681602 (NC_000011.10:75295221:AA: 7140/26754) Row 84681603 (NC_000011.10:75295221:A: 2749/26754) Row 84681604 (NC_000011.10:75295221::A 125/26754)...	-	Oct 16, 2022 (156)
68	14KJPN Submission ignored due to conflicting rows: Row 84681602 (NC_000011.10:75295221:AA: 7140/26754) Row 84681603 (NC_000011.10:75295221:A: 2749/26754) Row 84681604 (NC_000011.10:75295221::A 125/26754)...	-	Oct 16, 2022 (156)
69	14KJPN Submission ignored due to conflicting rows: Row 84681602 (NC_000011.10:75295221:AA: 7140/26754) Row 84681603 (NC_000011.10:75295221:A: 2749/26754) Row 84681604 (NC_000011.10:75295221::A 125/26754)...	-	Oct 16, 2022 (156)
70	14KJPN Submission ignored due to conflicting rows: Row 84681602 (NC_000011.10:75295221:AA: 7140/26754) Row 84681603 (NC_000011.10:75295221:A: 2749/26754) Row 84681604 (NC_000011.10:75295221::A 125/26754)...	-	Oct 16, 2022 (156)
71	TopMed	NC_000011.10 - 75295222	Apr 26, 2021 (155)
72	ALFA	NC_000011.10 - 75295222	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)
rs71467803	Oct 14, 2011 (136)
rs140788910	Sep 17, 2011 (135)
rs398016688	Aug 21, 2014 (142)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
106356156, ss4890810500	NC_000011.10:75295221:AAAAAAAAAAAA… NC_000011.10:75295221:AAAAAAAAAAAAAA:	NC_000011.10:75295221:AAAAAAAAAAAA… NC_000011.10:75295221:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA	(self)
13787542407	NC_000011.10:75295221:AAAAAAAAAAAA… NC_000011.10:75295221:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA	NC_000011.10:75295221:AAAAAAAAAAAA… NC_000011.10:75295221:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA	(self)
ss4237952467	NC_000011.10:75295221:AAAAAAAAAAAA… NC_000011.10:75295221:AAAAAAAAAAAAA:	NC_000011.10:75295221:AAAAAAAAAAAA… NC_000011.10:75295221:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
13787542407	NC_000011.10:75295221:AAAAAAAAAAAA… NC_000011.10:75295221:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	NC_000011.10:75295221:AAAAAAAAAAAA… NC_000011.10:75295221:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
13787542407	NC_000011.10:75295221:AAAAAAAAAAAA… NC_000011.10:75295221:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	NC_000011.10:75295221:AAAAAAAAAAAA… NC_000011.10:75295221:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss4237952466	NC_000011.10:75295221:AAAAAAAAAA:	NC_000011.10:75295221:AAAAAAAAAAAA… NC_000011.10:75295221:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
13787542407	NC_000011.10:75295221:AAAAAAAAAAAA… NC_000011.10:75295221:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	NC_000011.10:75295221:AAAAAAAAAAAA… NC_000011.10:75295221:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
13787542407	NC_000011.10:75295221:AAAAAAAAAAAA… NC_000011.10:75295221:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	NC_000011.10:75295221:AAAAAAAAAAAA… NC_000011.10:75295221:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
13787542407	NC_000011.10:75295221:AAAAAAAAAAAA… NC_000011.10:75295221:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	NC_000011.10:75295221:AAAAAAAAAAAA… NC_000011.10:75295221:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss4237952465	NC_000011.10:75295221:AAAAAAA:	NC_000011.10:75295221:AAAAAAAAAAAA… NC_000011.10:75295221:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
13787542407	NC_000011.10:75295221:AAAAAAAAAAAA… NC_000011.10:75295221:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	NC_000011.10:75295221:AAAAAAAAAAAA… NC_000011.10:75295221:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss4237952464	NC_000011.10:75295221:AAAAA:	NC_000011.10:75295221:AAAAAAAAAAAA… NC_000011.10:75295221:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
13787542407	NC_000011.10:75295221:AAAAAAAAAAAA… NC_000011.10:75295221:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	NC_000011.10:75295221:AAAAAAAAAAAA… NC_000011.10:75295221:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss3692097418, ss4237952463	NC_000011.10:75295221:AAAA:	NC_000011.10:75295221:AAAAAAAAAAAA… NC_000011.10:75295221:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
13787542407	NC_000011.10:75295221:AAAAAAAAAAAA… NC_000011.10:75295221:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	NC_000011.10:75295221:AAAAAAAAAAAA… NC_000011.10:75295221:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
ss3008358843, ss5202725589	NC_000011.9:75006265:AAA:	NC_000011.10:75295221:AAAAAAAAAAAA… NC_000011.10:75295221:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
ss4237952462, ss5287989861	NC_000011.10:75295221:AAA:	NC_000011.10:75295221:AAAAAAAAAAAA… NC_000011.10:75295221:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
13787542407	NC_000011.10:75295221:AAAAAAAAAAAA… NC_000011.10:75295221:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	NC_000011.10:75295221:AAAAAAAAAAAA… NC_000011.10:75295221:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
ss3692097417	NC_000011.10:75295222:AAA:	NC_000011.10:75295221:AAAAAAAAAAAA… NC_000011.10:75295221:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
ss83156037	NC_000011.8:74683936:AA:	NC_000011.10:75295221:AAAAAAAAAAAA… NC_000011.10:75295221:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3832704157, ss5202725587	NC_000011.9:75006265:AA:	NC_000011.10:75295221:AAAAAAAAAAAA… NC_000011.10:75295221:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3063697944, ss3064523294, ss4237952461, ss5287989859, ss5483088975, ss5750844498	NC_000011.10:75295221:AA:	NC_000011.10:75295221:AAAAAAAAAAAA… NC_000011.10:75295221:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
13787542407	NC_000011.10:75295221:AAAAAAAAAAAA… NC_000011.10:75295221:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	NC_000011.10:75295221:AAAAAAAAAAAA… NC_000011.10:75295221:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3692097416	NC_000011.10:75295223:AA:	NC_000011.10:75295221:AAAAAAAAAAAA… NC_000011.10:75295221:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss5202725588	NC_000011.9:75006265:A:	NC_000011.10:75295221:AAAAAAAAAAAA… NC_000011.10:75295221:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4237952460, ss5287989857, ss5483088976, ss5750844499	NC_000011.10:75295221:A:	NC_000011.10:75295221:AAAAAAAAAAAA… NC_000011.10:75295221:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
13787542407	NC_000011.10:75295221:AAAAAAAAAAAA… NC_000011.10:75295221:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	NC_000011.10:75295221:AAAAAAAAAAAA… NC_000011.10:75295221:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3692097415	NC_000011.10:75295224:A:	NC_000011.10:75295221:AAAAAAAAAAAA… NC_000011.10:75295221:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss39986051	NT_167190.1:20312060:A:	NC_000011.10:75295221:AAAAAAAAAAAA… NC_000011.10:75295221:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss294710209	NC_000011.8:74683914::A	NC_000011.10:75295221:AAAAAAAAAAAA… NC_000011.10:75295221:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss294710210	NC_000011.8:74683938::A	NC_000011.10:75295221:AAAAAAAAAAAA… NC_000011.10:75295221:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss5202725590	NC_000011.9:75006265::A	NC_000011.10:75295221:AAAAAAAAAAAA… NC_000011.10:75295221:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4237952453, ss5287989858, ss5483088977, ss5750844500	NC_000011.10:75295221::A	NC_000011.10:75295221:AAAAAAAAAAAA… NC_000011.10:75295221:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
13787542407	NC_000011.10:75295221:AAAAAAAAAAAA… NC_000011.10:75295221:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000011.10:75295221:AAAAAAAAAAAA… NC_000011.10:75295221:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3692097414	NC_000011.10:75295225::A	NC_000011.10:75295221:AAAAAAAAAAAA… NC_000011.10:75295221:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss39935628	NT_167190.1:20312060::A	NC_000011.10:75295221:AAAAAAAAAAAA… NC_000011.10:75295221:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss95573107	NT_167190.1:20312085::A	NC_000011.10:75295221:AAAAAAAAAAAA… NC_000011.10:75295221:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4237952454, ss5287989860, ss5750844502	NC_000011.10:75295221::AA	NC_000011.10:75295221:AAAAAAAAAAAA… NC_000011.10:75295221:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
13787542407	NC_000011.10:75295221:AAAAAAAAAAAA… NC_000011.10:75295221:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000011.10:75295221:AAAAAAAAAAAA… NC_000011.10:75295221:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4237952455	NC_000011.10:75295221::AAA	NC_000011.10:75295221:AAAAAAAAAAAA… NC_000011.10:75295221:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
13787542407	NC_000011.10:75295221:AAAAAAAAAAAA… NC_000011.10:75295221:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000011.10:75295221:AAAAAAAAAAAA… NC_000011.10:75295221:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4237952456	NC_000011.10:75295221::AAAA	NC_000011.10:75295221:AAAAAAAAAAAA… NC_000011.10:75295221:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
13787542407	NC_000011.10:75295221:AAAAAAAAAAAA… NC_000011.10:75295221:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000011.10:75295221:AAAAAAAAAAAA… NC_000011.10:75295221:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4237952457	NC_000011.10:75295221::AAAAA	NC_000011.10:75295221:AAAAAAAAAAAA… NC_000011.10:75295221:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
13787542407	NC_000011.10:75295221:AAAAAAAAAAAA… NC_000011.10:75295221:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000011.10:75295221:AAAAAAAAAAAA… NC_000011.10:75295221:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4237952458	NC_000011.10:75295221::AAAAAA	NC_000011.10:75295221:AAAAAAAAAAAA… NC_000011.10:75295221:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4237952459	NC_000011.10:75295221::AAAAAAA	NC_000011.10:75295221:AAAAAAAAAAAA… NC_000011.10:75295221:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)

Removed from this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Destination RSIDs
ss3149586058	NC_000011.10:75295221:AAAAAAAA:	NC_000011.10:75295221:AAAAAAAAAAAA… NC_000011.10:75295221:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA
ss3149586059	NC_000011.10:75295221:AAAAAAAAA:	NC_000011.10:75295221:AAAAAAAAAAAA… NC_000011.10:75295221:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA

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

No publications for rs34666904

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

rs34666904