Original source

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

Alleles
A/T | Ancestral: A | Ambiguity code: W
Location

Chromosome X:48687242 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

X:g.48687242A>T

Genotyping chips

This variation has assays on: Illumina_HumanOmni1-Quad

Variation displays