Original source

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

Alleles
-/G
Location

Chromosome X: between 136145604 and 136145605 (forward strand) | View in location tab

Most severe consequence
HGVS name

X:g.136145604_136145605insG

About this variant

This variant overlaps 10 transcripts.

Variation displays