Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs104893877
rs104893877
0.010 GeneticVariation BEFREE Astrocytes have a neuroprotective role in several detrimental brain conditions; we therefore analyzed the effects of the overexpression of wild-type α-synuclein and its A30P and A53T mutants on autophagy and apoptosis. 28573674

2018

dbSNP: rs104893878
rs104893878
0.010 GeneticVariation BEFREE Astrocytes have a neuroprotective role in several detrimental brain conditions; we therefore analyzed the effects of the overexpression of wild-type α-synuclein and its A30P and A53T mutants on autophagy and apoptosis. 28573674

2018

dbSNP: rs12524487
rs12524487
0.010 GeneticVariation BEFREE Our findings indicated that rs12524487 in HLA-B/MICA was a genetic risk factor for TA in a Chinese Han population and rs9366782 in this region was associated with ischemic brain disease in TA but not TA susceptibility. 28261975

2018

dbSNP: rs1280914556
rs1280914556
0.010 GeneticVariation BEFREE Astrocytes have a neuroprotective role in several detrimental brain conditions; we therefore analyzed the effects of the overexpression of wild-type α-synuclein and its A30P and A53T mutants on autophagy and apoptosis. 28573674

2018

dbSNP: rs756915170
rs756915170
0.010 GeneticVariation BEFREE Astrocytes have a neuroprotective role in several detrimental brain conditions; we therefore analyzed the effects of the overexpression of wild-type α-synuclein and its A30P and A53T mutants on autophagy and apoptosis. 28573674

2018

dbSNP: rs9366782
rs9366782
0.010 GeneticVariation BEFREE Our findings indicated that rs12524487 in HLA-B/MICA was a genetic risk factor for TA in a Chinese Han population and rs9366782 in this region was associated with ischemic brain disease in TA but not TA susceptibility. 28261975

2018

dbSNP: rs961750842
rs961750842
0.010 GeneticVariation BEFREE Astrocytes have a neuroprotective role in several detrimental brain conditions; we therefore analyzed the effects of the overexpression of wild-type α-synuclein and its A30P and A53T mutants on autophagy and apoptosis. 28573674

2018

dbSNP: rs1333049
rs1333049
0.010 GeneticVariation BEFREE We failed to validate the association of <i>CDKN2B-AS1</i> rs1333049 with the risk of brain disease. 28138111

2017

dbSNP: rs2016520
rs2016520
0.010 GeneticVariation BEFREE PPARD rs2016520 polymorphism and circulating lipid levels connect with brain diseases in Han Chinese and suggest sex-dependent effects. 25776471

2015

dbSNP: rs2433322
rs2433322
0.010 GeneticVariation BEFREE Our genetic association study only offered evidence for susceptibility of PDLIM5 to bipolar disorder, but the positive SNP rs2433322 could not indicate a direct cause of this complicated brain disorder. 19448850

2009