Original source

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

Alleles
G/A | Ambiguity code: R | MAF: 0.20 (A)
Location

Chromosome 12:106356479 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

12:g.106356479G>A

Variation displays