Original source

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

Alleles
T/C | Ancestral: T | Ambiguity code: Y
Location

Chromosome 17:34429665 (forward strand) | View in location tab

Co-located

with dbSNP rs111626093 (C/T)

Most severe consequence
Evidence status

HGVS name

17:g.34429665T>C

Variation displays