Original source

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

Alleles
A/- | Ancestral: A
Location

Chromosome X:135984286 (forward strand) | View in location tab

Most severe consequence
HGVS name

X:g.135984286delA

About this variant

This variant overlaps 4 transcripts.

Variation displays