rs933399
This variant is located in the PHETA1 gene.
▶Research that mentions this SNP (1)
▶Linkage disequilibrium mapping of bipolar affective disorder at 12q23‐q24 provides evidence for association at CUX2 and FLJ32356AssociationN=721Beate Glaser et al.(2005)· American Journal of Medical Genetics Part B: Neuropsychiatric Genetics
This LD mapping study identified significant associations between bipolar affective disorder and genetic markers on chromosome 12q23-q24. Two SNPs (rs3847953, P=0.002 and rs933399, P=0.004) and an insertion/deletion (rs3840795, P=0.005) in regions containing CUX2 and FLJ32356 genes showed significant association after Bonferroni correction in 347 bipolar cases and 374 controls.
About PHETA1
This gene encodes a protein that localizes to the endosome and interacts with the enzyme, inositol polyphosphate 5-phosphatase OCRL-1. Alternate splicing results in multiple transcript variants. [provided by RefSeq, May 2010]
View all PHETA1 variants →Gene information from NCBI Gene. Variant classifications from ClinVar.
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