Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
T/- | Ancestral: T
Location

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

Co-located

with dbSNP rs79547075 (T/C)

Most severe consequence
HGVS name

17:g.34355076delT

About this variant

This variant overlaps 3 transcripts.

Variation displays