Original source

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

Alleles
T/A|Ancestral: T|Ambiguity code: W|MAF: 0.38 (A)
Location

Chromosome X:120456678 (forward strand)|View in location tab

Most severe consequence
 
Synonymous variant
Evidence status

Clinical significance

HGVS names

This variant has 14 HGVS names - Show

Genotyping chips

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

About this variant

This variant overlaps 6 transcripts, 1 regulatory feature, has 3988 sample genotypes and is associated with 2 phenotypes.

Variant displays