Original source

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

Alleles
C/A | Ancestral: C | Ambiguity code: M
Location

Chromosome 12:120875018 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

12:g.120875018C>A

Variation displays