Original source

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

T/G | Ancestral: G | Ambiguity code: K | MAF: 0.22 (T)

Chromosome 20:766241 (forward strand) | View in location tab

Most severe consequence
Non coding transcript exon variant
Evidence status


Archive dbSNP rs57849739

HGVS names

This variant has 5 HGVS names - Show

About this variant

This variant overlaps 5 transcripts and has 3110 sample genotypes.

Variant displays