Original source

Variants (including SNPs and indels) imported from dbSNP (release 136)|View in dbSNP

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

Chromosome 4:80833674 (forward strand)|View in location tab

Most severe consequence
 
Intergenic variant
HGVS name

4:g.80833674A>C

About this variant

This variant has 1 sample genotype.

Variant displays