Original source

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

Alleles
A/G | Ancestral: A | Ambiguity code: R | MAF: 0.01 (G)
Location

Chromosome 12:51186442 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

12:g.51186442A>G

Variation displays