Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

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

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

Most severe consequence
 
Upstream gene variant
HGVS name

17:g.80168167C>T

About this variant

This variant overlaps 6 transcripts.

Variant displays