Original source

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

Alleles
A/C | Ancestral: C | Ambiguity code: M | MAF: 0.23 (C)
Location

Chromosome 12:106355830 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

12:g.106355830A>C

Variation displays