Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R | MAF: 0.42 (A)
Location

Chromosome X:142205575 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms
HGVS name

X:g.142205575G>A

Genotyping chips

This variation has assays on: Illumina_HumanOmni1-Quad, HumanOmniExpress, Illumina_HumanOmni2.5

Variation displays