Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
G/A | Ancestral: G | Ambiguity code: R
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_HumanOmni2.5, Illumina_HumanOmni1-Quad, HumanOmniExpress

About this variant

This variant overlaps 1 transcript and has 330 individual genotypes.

Variation displays