Original source

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

Alleles
G/C|Ancestral: G|Ambiguity code: S|MAF: 0.13 (C)
Location

Chromosome 9:124450522 (forward strand)|View in location tab

Most severe consequence
 
Upstream gene variant
Evidence status

HGVS name

9:g.124450522G>C

About this variant

This variant overlaps 2 transcripts and has 2505 sample genotypes.

Variant displays