Original source

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

G/T | Ancestral: G | Ambiguity code: K

Chromosome 3:170996771 (forward strand) | View in location tab

Most severe consequence
3 prime UTR variant
Evidence status


Archive dbSNP rs62623382

HGVS names

This variant has 2 HGVS names - Show

About this variant

This variant overlaps 4 transcripts and 1 regulatory feature.

Variant displays