Original source

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

Alleles
T/C | Ancestral: T | Ambiguity code: Y | MAF: 0.05 (C)
Location

Chromosome 20:45336361 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

20:g.45336361T>C

Variation displays