Original source

Variants (including SNPs and indels) imported from dbSNP (release 138) | View in dbSNP

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

Chromosome 12:6643070 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

12:g.6643070T>G

Variation displays