Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 274
Gene Symbol: BIN1
BIN1
CUI: C1270972
Disease: Mild cognitive disorder
Mild cognitive disorder
0.320 GeneticVariation BEFREE In the present study, we investigated the association of genetic polymorphisms of five genes (8-oxoguanine DNA glycosylase 1 (OGG1), bridging integrator 1 (BIN1), sortilin-related receptor 1 (SORL1), presenilin 2 (PSEN2) and nerve growth factor (NGF)) with MCI risk in a Xinjiang Uygur population. 30983028

2019

Entrez Id: 274
Gene Symbol: BIN1
BIN1
CUI: C1270972
Disease: Mild cognitive disorder
Mild cognitive disorder
0.320 GeneticVariation BEFREE To evaluate cognitive performance and presence of polymorphisms of the genes SORL1(rs11218304), PVRL2(rs6859), CR1(rs6656401), TOMM40(rs2075650), APOE (isoforms ɛ2, ɛ3, ɛ4), PICALM(rs3851179), GWAS_14q(rs11622883), BIN1(rs744373), and CLU (rs227959 and rs11136000) in patients with MCI and healthy individuals. 30503753

2018

Entrez Id: 274
Gene Symbol: BIN1
BIN1
CUI: C1270972
Disease: Mild cognitive disorder
Mild cognitive disorder
0.320 Biomarker CTD_human To evaluate cognitive performance and presence of polymorphisms of the genes SORL1(rs11218304), PVRL2(rs6859), CR1(rs6656401), TOMM40(rs2075650), APOE (isoforms ɛ2, ɛ3, ɛ4), PICALM(rs3851179), GWAS_14q(rs11622883), BIN1(rs744373), and CLU (rs227959 and rs11136000) in patients with MCI and healthy individuals. 30503753

2018