Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

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

Chromosome X:71117448 (forward strand)|View in location tab

Most severe consequence
 
Upstream gene variant
HGVS name

X:g.71117448T>G

About this variant

This variant overlaps 4 transcripts.

Variant displays