Original source

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

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

Chromosome X:43653054 (forward strand) | View in location tab

Most severe consequence
 
Upstream gene variant
Evidence status

HGVS name

X:g.43653054G>C

About this variant

This variant overlaps 3 transcripts and has 7 sample genotypes.

Variant displays