Original source

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

Alleles
A/G | Ambiguity code: R | MAF: 0.34 (A)
Location

Chromosome 12:52314267 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

12:g.52314267A>G

Variation displays