Original source

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

G/A | Ancestral: G | Ambiguity code: R | MAF: 0.20 (A)

Chromosome 3:49664550 (forward strand) | View in location tab

Most severe consequence
Synonymous variant
Evidence status


Archive dbSNP rs56540553, rs57210211

HGVS names

This variant has 3 HGVS names - Show

Genotyping chips

This variant has assays on 10 chips - Show

About this variant

This variant overlaps 2 transcripts, has 4071 sample genotypes, is associated with 4 phenotypes and is mentioned in 42 citations.

Variant displays