Original source

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

Alleles
T/G | Ancestral: T | Ambiguity code: K
Location

Chromosome X:136145527 (forward strand) | View in location tab

Most severe consequence
 
Upstream gene variant
HGVS name

X:g.136145527T>G

About this variant

This variant overlaps 10 transcripts.

Variant displays