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:154536951 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs59845413, rs17336780

This variant has 12 HGVS names - click the plus to show

Genotyping chips

This variant has assays on: Affy GenomeWideSNP_6.0, Illumina_CytoSNP12v1, Illumina_HumanOmni5

About this variant

This variant overlaps 14 transcripts, has 1513 sample genotypes and is mentioned in 2 citations.

Variant displays