Original source

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

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

Chromosome 16:47460872 (forward strand) | View in location tab

Most severe consequence
Synonymous variant
Evidence status

HGVS names

This variant has 10 HGVS names - Show

About this variant

This variant overlaps 30 transcripts and 1 regulatory feature.

Variant displays