Original source

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

Alleles
G/T | Ancestral: G | Ambiguity code: K
Location

Chromosome 17:34254373 (forward strand) | View in location tab

Most severe consequence
 
Upstream gene variant
HGVS name

17:g.34254373G>T

About this variant

This variant overlaps 4 transcripts and 1 regulatory feature.

Variant displays