Original source

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

A/G | Ancestral: G | Ambiguity code: R

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

Most severe consequence
Intergenic variant
Evidence status

HGVS name


This variant has assays on 4 chips - click the plus to show

About this variant

This variant has 1252 sample genotypes and is mentioned in 3 citations.

Variant displays