Original source

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

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

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

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs58620769

HGVS names

This variant has 15 HGVS names - Show

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