Original source

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

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

Chromosome 2:27309614 (forward strand) | View in location tab

Most severe consequence
3 prime UTR variant
Evidence status


Archive dbSNP rs3189969

HGVS names

This variant has 8 HGVS names - Show

About this variant

This variant overlaps 25 transcripts and has 1 sample genotype.

Variant displays