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:48682045 (forward strand) | View in location tab

Most severe consequence

This variation has 3 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_HumanOmni5

About this variant

This variant overlaps 6 transcripts.

Variation displays