Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | View in dbSNP

Alleles
A/G | Ancestral: G | Ambiguity code: R | MAF: 0.27 (A)
Location

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

Most severe consequence
Evidence status

HGVS name

X:g.125567397A>G

Genotyping chips

This variation has assays on: HumanOmniExpress, Illumina_HumanOmni2.5, Illumina_1M-duo

Variation displays