Original source

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

Alleles
A/G | Ancestral: A | Ambiguity code: R
Location

Chromosome X:136145126 (forward strand) | View in location tab

Most severe consequence
 
Upstream gene variant
HGVS name

X:g.136145126A>G

About this variant

This variant overlaps 10 transcripts.

Variant displays