Original source

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

Alleles
C/G | Ancestral: C | Ambiguity code: S | MAF: 0.35 (G)
Location

Chromosome 12:52314189 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

12:g.52314189C>G

Variation displays