Original source

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

Alleles
C/T | Ancestral: T | Ambiguity code: Y | MAF: 0.02 (T)
Location

Chromosome X:141293806 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

X:g.141293806C>T

Genotyping chips

This variation has assays on: Illumina_1M-duo, Illumina_HumanOmni1-Quad, Illumina_HumanOmni2.5

Variation displays