Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

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

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

Co-located

with dbSNP rs534064919 (C/-)

Most severe consequence
 
Missense variant

This variant has 3 HGVS names - click the plus to show

About this variant

This variant overlaps 1 transcript and 1 regulatory feature.

Variant displays