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:18896078 (forward strand) | View in location tab

Most severe consequence
 
Non coding transcript exon variant
| See all predicted consequences [Genes and regulation]
Evidence status

This variation has 6 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_Human1M-duo

About this variant

This variant overlaps 11 transcripts and has 258 individual genotypes.

Variation displays