Original source

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

Alleles
C/A|Ancestral: C|Ambiguity code: M
Location

Chromosome 4:73981878 (forward strand)|View in location tab

Co-located variant

dbSNP rs534064919 (C/-)

Most severe consequence
 
Missense variant
HGVS names

This variant has 3 HGVS names - Show

About this variant

This variant overlaps 1 transcript and 1 regulatory feature.

Variant displays