Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | View in dbSNP

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

Chromosome 17:80168167 (forward strand) | View in location tab

Most severe consequence
HGVS name

17:g.80168167C>T

Variation displays