Original source

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

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

Chromosome 1:158420876 (forward strand) | View in location tab

Most severe consequence
 
Upstream gene variant
HGVS name

1:g.158420876A>C

About this variant

This variant overlaps 1 transcript and has 269 sample genotypes.

Variant displays