Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y
Location

Chromosome X:3603882 (forward strand) | View in location tab

Most severe consequence
 
Downstream gene variant
HGVS name

X:g.3603882C>T

Genotyping chips

This variant has assays on: Illumina_HumanOmni5

About this variant

This variant overlaps 3 transcripts.

Variant displays