Original source

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

G/A | Ancestral: G | Ambiguity code: R | MAF: 0.47 (A)

Chromosome 20:44111265 (forward strand) | View in location tab

Most severe consequence
Downstream gene variant
Evidence status


Archive dbSNP rs56853691

HGVS names

This variant has 2 HGVS names - Show

About this variant

This variant overlaps 2 transcripts and has 2509 sample genotypes.

Variant displays