Original source

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

Alleles
T/C | Ancestral: C | Ambiguity code: Y | MAF: 0.03 (C)
Location

Chromosome 20:57226319 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

20:g.57226319T>C

Variation displays