rs7865618, CDKN2B-AS1

N. diseases: 11
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
0.820 GeneticVariation BEFREE The results indicated a significant association between the presence of risk alleles of rs7865618 and CHD in the TLGS population (P = 0.03; OR: 1.73; CI95%: 1.04 - 2.88). 28287809 2017
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
0.820 GeneticVariation BEFREE In addition, rs7865618 was associated with an 8.10-fold increased risk of CHD in women under a recessive model (OR = 8.10, 95% CI: 1.74-37.68, P = 0.006). 27741513 2016
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
0.820 GeneticVariation GWASDB A genome-wide association study identifies LIPA as a susceptibility gene for coronary artery disease. 21606135 2011
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
0.820 GeneticVariation GWASCAT A genome-wide association study identifies LIPA as a susceptibility gene for coronary artery disease. 21606135 2011
Glaucoma, Open-Angle
CUI: C0017612
Disease: Glaucoma, Open-Angle
0.800 GeneticVariation GWASDB Common variants in CDKN2B-AS1 associated with optic-nerve vulnerability of glaucoma identified by genome-wide association studies in Japanese. 22428042 2012
Glaucoma, Open-Angle
CUI: C0017612
Disease: Glaucoma, Open-Angle
0.800 GeneticVariation GWASDB Common variants at 9p21 and 8q22 are associated with increased susceptibility to optic nerve degeneration in glaucoma. 22570617 2012
Glaucoma, Open-Angle
CUI: C0017612
Disease: Glaucoma, Open-Angle
0.800 GeneticVariation GWASCAT Common variants in CDKN2B-AS1 associated with optic-nerve vulnerability of glaucoma identified by genome-wide association studies in Japanese. 22428042 2012
Calcification of coronary artery
CUI: C1611184
Disease: Calcification of coronary artery
0.700 GeneticVariation GWASDB Risk loci for coronary artery calcification replicated at 9p21 and 6q24 in the Heinz Nixdorf Recall Study. 23394302 2013
Glaucoma
CUI: C0017601
Disease: Glaucoma
0.700 GeneticVariation GWASDB Common variants on chromosome 9p21 are associated with normal tension glaucoma. 22792221 2012
Calcification of coronary artery
CUI: C1611184
Disease: Calcification of coronary artery
0.700 GeneticVariation GWASDB Genome-wide association study for coronary artery calcification with follow-up in myocardial infarction. 22144573 2011
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
0.700 GeneticVariation GWASDB Genomewide association analysis of coronary artery disease. 17634449 2007
Seizures
CUI: C0036572
Disease: Seizures
0.010 GeneticVariation BEFREE The occurrence of bleeding was associated with the TT genotype and T allele of rs1333040, while the presence of seizures appeared associated with the GG genotype of rs7865618. 24820060 2014
Congenital arteriovenous malformation
CUI: C0003857
Disease: Congenital arteriovenous malformation
0.010 GeneticVariation BEFREE Association between polymorphisms rs1333040 and rs7865618 of chromosome 9p21 and sporadic brain arteriovenous malformations. 24820060 2014
Arteriovenous hemangioma
CUI: C0334533
Disease: Arteriovenous hemangioma
0.010 GeneticVariation BEFREE Association between polymorphisms rs1333040 and rs7865618 of chromosome 9p21 and sporadic brain arteriovenous malformations. 24820060 2014
Diabetes Mellitus
CUI: C0011849
Disease: Diabetes Mellitus
0.010 GeneticVariation BEFREE Finally, evidence was provided to suggest dual association of rs7865618 with MI and diabetes. 21511257 2011
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
0.010 GeneticVariation BEFREE Finally, evidence was provided to suggest dual association of rs7865618 with MI and diabetes. 21511257 2011
Diabetes
CUI: C0011847
Disease: Diabetes
0.010 GeneticVariation BEFREE Finally, evidence was provided to suggest dual association of rs7865618 with MI and diabetes. 21511257 2011