Original source

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

T/A | Ancestral: T | Ambiguity code: W | MAF: 0.03 (T)

Chromosome 16:46682524 (forward strand) | View in location tab

Most severe consequence
3 prime UTR variant
Evidence status


Archive dbSNP rs58762896

HGVS names

This variant has 7 HGVS names - Show

About this variant

This variant overlaps 10 transcripts and has 2778 sample genotypes.

Variant displays