Original source

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

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

Chromosome 12:6840888 (forward strand) | View in location tab

Most severe consequence
5 prime UTR variant
Evidence status


Archive dbSNP rs2234963

HGVS names

This variant has 5 HGVS names - Show

About this variant

This variant overlaps 21 transcripts, has 2505 sample genotypes and is mentioned in 2 citations.

Variant displays