Original source

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

Alleles
T/G | Ancestral: G | Ambiguity code: K | MAF: 0.04 (G)
Location

Chromosome 12:6533904 (forward strand) | View in location tab

Most severe consequence
 
Upstream gene variant
Evidence status

HGVS name

12:g.6533904T>G

About this variant

Variant displays