Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

G/T | Ancestral: G | Ambiguity code: K | MAF: 0.20 (T)

Chromosome 4:53378156 (forward strand) | View in location tab

Most severe consequence
Non coding transcript exon variant
Evidence status


Archive dbSNP rs61522860, rs3811784

This variant has 9 HGVS names - click the plus to show

About this variant

Variant displays