Original source

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

Alleles
G/C | Ancestral: G | Ambiguity code: S
Location

Chromosome X:48686211 (forward strand) | View in location tab

Most severe consequence
 
Intron variant

This variant has 8 HGVS names - click the plus to show

Genotyping chips

This variant has assays on: Illumina_HumanOmni1-Quad

About this variant

This variant overlaps 8 transcripts and has 269 sample genotypes.

Variant displays