Original source

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

Alleles
G/A | Ancestral: T | Ambiguity code: R
Location

Chromosome X:9736084 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

This variant has 2 HGVS names - click the plus to show

Genotyping chips

This variant has assays on: Affy GenomeWideSNP_6.0

About this variant

This variant overlaps 3 transcripts and has 684 sample genotypes.

Variant displays