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: 0.09 (G)
Location

Chromosome X:120425707 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

X:g.120425707A>G

Genotyping chips

This variation has assays on: Illumina_HumanOmni1-Quad

Variation displays