Original source

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

Alleles
A/G|Ancestral: A|Ambiguity code: R|MAF: 0.29 (G)
Location

Chromosome 9:129664494 (forward strand)|View in location tab

Most severe consequence
 
Upstream gene variant
Evidence status

HGVS name

9:g.129664494A>G

About this variant

This variant overlaps 1 transcript and has 2509 sample genotypes.

Variant displays