Original source

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

Alleles
T/-|Ancestral: T
Location

Chromosome 17:34355076 (forward strand)|View in location tab

Co-located variant

dbSNP rs79547075 (T/C)

Most severe consequence
 
Upstream gene variant
Evidence status

HGVS name

17:g.34355076delT

About this variant

This variant overlaps 2 transcripts and 1 regulatory feature.

Variant displays