Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

Alleles
T/G | Ancestral: G | Ambiguity code: K | MAF: 0.02 (G)
Location

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

Most severe consequence
Evidence status

HGVS name

12:g.6533904T>G

Variation displays