Original source

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

A/G|Ancestral: G|Ambiguity code: R|MAF: 0.28 (A)

Chromosome X:125567397 (forward strand)|View in location tab

Most severe consequence
Intergenic variant
Evidence status

HGVS name


Genotyping chips

This variant has assays on 4 chips - Show

About this variant

This variant has 3756 sample genotypes and is mentioned in 3 citations.

Variant displays