Original source

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

Alleles
-/T
Location

Chromosome 7: between 100718932 and 100718933 (forward strand) | View in location tab

Most severe consequence
 
Upstream gene variant
HGVS name

7:g.100718932_100718933insT

About this variant

This variant overlaps 1 transcript.

Variant displays