Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.30 (C)
Location

Chromosome 12:52313829 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

12:g.52313829C>T

Variation displays