Original source

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

Alleles
-/T
Location

Chromosome 2: between 112829750 and 112829751 (forward strand) | View in location tab

Most severe consequence
 
Downstream gene variant
HGVS name

2:g.112829750_112829751insT

About this variant

This variant overlaps 7 transcripts.

Variant displays