Original source

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

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

Chromosome 4:73981890 (forward strand)|View in location tab

Most severe consequence
 
Synonymous variant
HGVS names

This variant has 3 HGVS names - Show

About this variant

This variant overlaps 1 transcript and 1 regulatory feature.

Variant displays