Original source

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

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

Chromosome X:151395309 (forward strand) | View in location tab

Most severe consequence
 
Upstream gene variant
HGVS name

X:g.151395309C>G

About this variant

This variant overlaps 3 transcripts.

Variant displays