Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1035071612
rs1035071612
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
0.060 GeneticVariation BEFREE Our data suggested that the polymorphism of LRP C766T was strongly associated with AD and T allele might be a protective factor for AD in Chinese Han population. 18706476

2008

dbSNP: rs1035071612
rs1035071612
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
0.060 GeneticVariation BEFREE In the present study, we have investigated the extent of amyloid beta protein (Abeta) deposition as cerebral amyloid angiopathy (CAA) or senile plaques (SP) in relationship to OLR1 +1071 and +1073 polymorphisms and LRP1 C766T polymorphism in patients with AD There was an increased Abeta40 load as CAA, but not as SP, in frontal cortex of AD patients carrying OLR1+1073 CC genotype, compared to those with CT, TT or CT+TT genotypes, but only in those individuals without apolipoprotein (APOE) epsilon4 allele. 16328515

2006

dbSNP: rs1035071612
rs1035071612
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
0.060 GeneticVariation BEFREE In addition, the C766T polymorphism was shown not to influence the age onset of AD. 15925094

2005

dbSNP: rs1035071612
rs1035071612
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
0.060 GeneticVariation BEFREE The C-allele of the silent C766T polymorphism in exon 3 of the LRP gene might be associated with AD, however, results are conflicting and thus discussed controversially. 12898587

2003

dbSNP: rs1035071612
rs1035071612
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
0.060 GeneticVariation BEFREE Recently, several studies have reported a correlation between a polymorphism (C766T) in exon 3 of LRP and AD. 10027548

1999

dbSNP: rs1035071612
rs1035071612
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
0.060 GeneticVariation BEFREE The LRP C766T polymorphism is protective against Alzheimer's disease, perhaps through alteration of LRP expression. 9832203

1998