Original source

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

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

Chromosome 13:27621390 (forward strand) | View in location tab

Most severe consequence
5 prime UTR variant
HGVS names

This variant has 5 HGVS names - Show

About this variant

This variant overlaps 11 transcripts and 1 regulatory feature.

Variant displays