SNP Report

Name	rs766288 dbSNP Ensembl
Location	Chrchr1:231557942(Forward)
Variant Alleles	G/T
Ancestral Allele	G
Annotation	regulatory_region_variant
Consequence to Transcript	regulatory_region_variant(ENST00000602634, ENST00000602956, ENST00000602962, ENST00000602885, ENST00000602567, ENST00000366639, ENST00000413309, ENST00000602825, ENST00000475168)
No. of Studies (Positive/Negative)	2 (2/0)

Reference	Research Type	Statistical Result	Relation Description
Okuda, 2010	patients and normal controls		We found an association between rs766288 in TSNAX and female...... We found an association between rs766288 in TSNAX and female MDD in the allele/genotype analysis. More...
Arias, 2014	Patients and nomal controls	p(genotype)=0.03; p(allele)=0.011	Rs3738401 (DISC1), rs1615409 and rs766288 (TSNAX) showed gen...... Rs3738401 (DISC1), rs1615409 and rs766288 (TSNAX) showed genotypic and allelic evidence of association with the risk of MDD (Supplementary Table 2). Logistic regression models controlled for age confirmed the association of these polymorphisms with MDD (Table 1). In detail, rs3738401 AA genotype, rs1615409 AA genotype and rs766288 T allele were associated with lower MDD risk(p=0.004; p=0.0019; p=0.008, respectively). More...

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Note:
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Genetic/Epigenetic Locus	Protein and Other Molecule	Cell and Molecular Pathway	Neural System	Cognition and Behavior	Symptoms and Signs	Environment	MDD

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