Original source

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

Alleles
G/C | Ancestral: G | Ambiguity code: S
Location

Chromosome X:48825656 (forward strand) | View in location tab

Most severe consequence
 
Upstream gene variant
HGVS name

X:g.48825656G>C

About this variant

This variant overlaps 9 transcripts.

Variant displays