Original source

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

Alleles
A/C | Ancestral: A | Ambiguity code: M | MAF: 0.16 (A)
Location

Chromosome 12:53190390 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs61599856, rs12818335

HGVS name

12:g.53190390A>C

Variation displays