Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

Alleles
G/A|Ancestral: G|Ambiguity code: R|MAF: 0.46 (G)
Location

Chromosome 9:22034720 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs58620769

HGVS names

This variant has 15 HGVS names - Hide

9:g.22034720G>A
ENST00000584020.5:n.261-12031G>A
ENST00000584816.5:n.261-12031G>A
ENST00000585267.5:n.372-12031G>A
ENST00000582301.5:n.261-12031G>A
ENST00000577551.5:n.261-12031G>A
ENST00000584637.5:n.261-12031G>A
ENST00000582072.5:n.261-12031G>A
ENST00000584351.5:n.846+1734G>A
ENST00000455933.6:n.68-12031G>A
ENST00000581051.5:n.261-12031G>A
ENST00000580467.5:n.372-12031G>A
ENST00000428597.5:n.846+1734G>A
ENST00000580576.5:n.533+5126G>A
ENST00000583719.5:n.372-12031G>A

Genotyping chips

This variant has assays on 6 chips - Show

About this variant

This variant overlaps 16 transcripts, has 3691 sample genotypes, is associated with 1 phenotype and is mentioned in 11 citations.

Variant displays