Original source

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

Alleles
A/T | Ancestral: A | Ambiguity code: W
Location

Chromosome X:48828832 (forward strand) | View in location tab

Most severe consequence
 
Upstream gene variant
HGVS name

X:g.48828832A>T

Genotyping chips

This variant has assays on: Illumina_HumanOmni1-Quad

About this variant

This variant overlaps 9 transcripts.

Variant displays