Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1107756
rs1107756
Entrez Id: 55198;387882
Gene Symbol: APPL2;C12orf75
APPL2;C12orf75
CUI: C0028754
Disease:
Obesity
0.010 GeneticVariation BEFREE We found significant evidence of association with overweight/obesity for rs2272495 and rs1107756. rs2272495 C allele and rs1107756 T allele both conferred a higher risk of being overweight and obese (OR 1.218, 95% CI 1.047-1.416, p = 0.011 for rs2272495; OR 1.166, 95% CI 1.014-1.341, p = 0.031 for rs1107756). 22462604 2012
dbSNP: rs2272495
rs2272495
Entrez Id: 55198
Gene Symbol: APPL2
APPL2
CUI: C0028754
Disease:
Obesity
0.010 GeneticVariation BEFREE After adjusting multiple comparisons, only the effect of rs227</span>2495</span> on overweight/o</span>besity remained to be significant (empirical p = 0.043). 22462604 2012
dbSNP: rs11112412
rs11112412
Entrez Id: 55198
Gene Symbol: APPL2
APPL2
CUI: C0011860
Disease:
Diabetes Mellitus, Non-Insulin-Dependent
0.010 GeneticVariation BEFREE The minor allele G of rs4640525 at APPL1 locus was protective from CAD in patients with T2DM, with the carriers of genotype CC at higher risk of CAD compared with non-carriers (OR = 2.830, 95%CI 1.285 - 6.230, P = 0.010; OR' = 4.992, 95%CI = 1.758 - 14.173, P' = 0.003, after adjustment for the other known CAD risk factors); the homozygotes of AA at rs11112412 in APPL2 gene had higher risk of CAD compared with those of GG (adjusted OR' = 5.697, 95%CI 1.006 - 32.257, P' = 0.049). 22340213 2011
dbSNP: rs11112412
rs11112412
Entrez Id: 55198
Gene Symbol: APPL2
APPL2
CUI: C1956346
Disease:
Coronary Artery Disease
0.010 GeneticVariation BEFREE The minor allele G of rs4640525 at APPL1 locus was protective from CAD in patients with T2DM, with the carriers of genotype CC at higher risk of CAD compared with non-carriers (OR = 2.830, 95%CI 1.285 - 6.230, P = 0.010; OR' = 4.992, 95%CI = 1.758 - 14.173, P' = 0.003, after adjustment for the other known CAD risk factors); the homozygotes of AA at rs11112412 in APPL2 gene had higher risk of CAD compared with those of GG (adjusted OR' = 5.697, 95%CI 1.006 - 32.257, P' = 0.049). 22340213 2011