Original source

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

Alleles
C/G | Ancestral: G | Ambiguity code: S | MAF: 0.39 (G)
Location

Chromosome 9:127212781 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

9:g.127212781C>G

Variation displays