Original source

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

Alleles
C/G | Ancestral: G | Ambiguity code: S | MAF: 0.40 (G)
Location

Chromosome 9:124450502 (forward strand) | View in location tab

Most severe consequence
 
Upstream gene variant
Evidence status

HGVS name

9:g.124450502C>G

About this variant

This variant overlaps 2 transcripts and has 2507 sample genotypes.

Variant displays