Original source

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

G/A/C | Ancestral: G | Ambiguity code: V

Chromosome 15:74720640 (forward strand) | View in location tab

Most severe consequence
Missense variant
Evidence status

HGVS names

This variant has 26 HGVS names - Show

About this variant

This variant overlaps 20 transcripts and is mentioned in 3 citations.

Variant displays