Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

Alleles
G/A|Ancestral: G|Ambiguity code: R|MAF: 0.10 (A)
Location

Chromosome X:154536951 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs59845413, rs17336780

HGVS names

This variant has 12 HGVS names - 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 4017 sample genotypes and is mentioned in 2 citations.

Variant displays