Original source

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

Alleles
T/C | Ancestral: C | Ambiguity code: Y | MAF: 0.01 (C)
Location

Chromosome 22:50568667 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

22:g.50568667T>C

Variation displays