Original source

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

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

Chromosome X:154061013 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

This variant has 13 HGVS names - click the plus to show

Genotyping chips

This variant has assays on: Illumina_Human1M-duo, Illumina_HumanOmni5

About this variant

This variant overlaps 13 transcripts, has 1188 sample genotypes and is mentioned in 1 citation.

Variant displays