Original source

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

Alleles
T/C | Ambiguity code: Y
Location

Chromosome 15:82825597 (forward strand) | View in location tab

Co-located

with dbSNP rs1267661 (C/T)

Most severe consequence
HGVS name

15:g.82825597T>C

Variation displays