Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1288987921
rs1288987921
Entrez Id: 322
Gene Symbol: APBB1
APBB1
CUI: C0002395
Disease:
Alzheimer's Disease 		0.010 GeneticVariation BEFREE Meta-analyses on AD association with BACE1 exon 5, BACE1 intron 5, FE65 intron 13, CYP46 intron 2, alpha(1)-antichymotrypsine Ala17Thr, bleomycin hydrolase I443V, lectin-like oxidized low-density lipoprotein receptor (OLR1) 3'-UTR (+1071) and (+1073), and very-low-density lipoprotein receptor (VLDLR) 5'-UTR (CGG-repeat) polymorphisms. 17854420 2008
dbSNP: rs368508811
rs368508811
Entrez Id: 322
Gene Symbol: APBB1
APBB1
CUI: C0002395
Disease:
Alzheimer's Disease 		0.010 GeneticVariation BEFREE Meta-analyses on AD association with BACE1 exon 5, BACE1 intron 5, FE65 intron 13, CYP46 intron 2, alpha(1)-antichymotrypsine Ala17Thr, bleomycin hydrolase I443V, lectin-like oxidized low-density lipoprotein receptor (OLR1) 3'-UTR (+1071) and (+1073), and very-low-density lipoprotein receptor (VLDLR) 5'-UTR (CGG-repeat) polymorphisms. 17854420 2008
dbSNP: rs4758416
rs4758416
Entrez Id: 322
Gene Symbol: APBB1
APBB1
CUI: C0028043
Disease:
Nicotine Dependence 		0.010 GeneticVariation BEFREE Individual SNP-based association analysis showed that all five SNPs are associated with at least one ND measure in one of the three samples; however, only the association of SNP rs4758416 with SQ and HSI remained significant after correction for multiple testing in the pooled sample. 18777128 2008