Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

Alleles
C/T|Ancestral: C|Ambiguity code: Y|MAF: < 0.01 (T)
Location

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

Most severe consequence
 
Downstream gene variant
Evidence status

HGVS name

X:g.3603882C>T

Genotyping chips

This variant has assays on: Illumina_HumanOmni5

About this variant

This variant overlaps 3 transcripts and has 2504 sample genotypes.

Variant displays