Original source

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

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

Chromosome 5:135027988 (forward strand) | View in location tab

Most severe consequence
3 prime UTR variant

Archive dbSNP rs3191669

HGVS names

This variant has 2 HGVS names - Show

About this variant

This variant overlaps 6 transcripts and 1 regulatory feature.

Variant displays