Original source

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

G/A | Ancestral: G | Ambiguity code: R

Chromosome 4:73982022 (forward strand) | View in location tab

Most severe consequence
5 prime UTR variant
Evidence status


Archive dbSNP rs3191278

HGVS names

This variant has 2 HGVS names - Show

About this variant

This variant overlaps 1 transcript, 1 regulatory feature and has 2 sample genotypes.

Variant displays