Original source

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

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

Chromosome X:48827199 (forward strand) | View in location tab

Most severe consequence
 
Upstream gene variant
HGVS name

X:g.48827199G>T

About this variant

This variant overlaps 10 transcripts.

Variant displays