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 | MAF: 0.02 (C)
Location

Chromosome 20:6767059 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

20:g.6767059T>C

Variation displays