Original source

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

Alleles
A/G | Ancestral: A | Ambiguity code: R
Location

Chromosome X:46911575 (forward strand) | View in location tab

Most severe consequence
 
Upstream gene variant
HGVS name

X:g.46911575A>G

Genotyping chips

This variant has assays on: Illumina_HumanOmni5

About this variant

This variant overlaps 4 transcripts.

Variant displays