Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.25 (C)
Location

Chromosome 20:35726051 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms
HGVS name

20:g.35726051C>T

Variation displays