Original source

Variants (including SNPs and indels) imported from dbSNP (release 139)|View in dbSNP

Alleles
C/A|Ambiguity code: M
Location

Chromosome 7:36989883 (forward strand)|View in location tab

Most severe consequence
 
Intergenic variant
HGVS name

7:g.36989883C>A

About this variant

This variant has 1 sample genotype.

Variant displays