Original source

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

Alleles
T/C|Ancestral: T|Ambiguity code: Y|MAF: 0.02 (C)
Location

Chromosome X:137564567 (forward strand)|View in location tab

Most severe consequence
 
Upstream gene variant
Evidence status

HGVS name

X:g.137564567T>C

Genotyping chips

This variant has assays on: Illumina_HumanOmni5

About this variant

Variant displays