Original source

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

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

Chromosome 12:106750257 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

12:g.106750257G>A

Variation displays