Original source

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

Alleles
T/C | Ancestral: T | Ambiguity code: Y
Location

Chromosome 12:120437284 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

12:g.120437284T>C

Variation displays