Source: CURATED

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs11154851
rs11154851
PDE7B ; LOC644135
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease 		0.800 GeneticVariation GWASDB Genome-wide association study of the rate of cognitive decline in Alzheimer's disease. 23535033

2014
dbSNP: rs11154851
rs11154851
PDE7B ; LOC644135
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease 		0.800 GeneticVariation GWASCAT Genome-wide association study of the rate of cognitive decline in Alzheimer's disease. 23535033

2014
dbSNP: rs10872447
rs10872447
PDE7B ; LOC101928373
CUI: C1304746
Disease: RDW - Red blood cell distribution width result
RDW - Red blood cell distribution width result 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370

2019
dbSNP: rs10872447
rs10872447
PDE7B ; LOC101928373
CUI: C0427460
Disease: Red cell distribution width determination
Red cell distribution width determination 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370

2019
dbSNP: rs12209685
rs12209685
PDE7B ; LOC101928373
CUI: C0005890
Disease: Body Height
Body Height 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370

2019
dbSNP: rs149647891
rs149647891
PDE7B
CUI: C0264408
Disease: Childhood asthma
Childhood asthma 		0.700 GeneticVariation GWASCAT Susceptibility to corticosteroid-induced adrenal suppression: a genome-wide association study. 29551627

2018
dbSNP: rs149647891
rs149647891
PDE7B
CUI: C0201968
Disease: Cortisol Measurement
Cortisol Measurement 		0.700 GeneticVariation GWASCAT Susceptibility to corticosteroid-induced adrenal suppression: a genome-wide association study. 29551627

2018
dbSNP: rs17835714
rs17835714
PDE7B
CUI: C0201899
Disease: Aspartate aminotransferase measurement
Aspartate aminotransferase measurement 		0.700 GeneticVariation GWASCAT Genome-Wide Association Study Identifies Loci for Liver Enzyme Concentrations in Mexican Americans: The GUARDIAN Consortium. 31219225

2019
dbSNP: rs2027518
rs2027518
PDE7B ; LOC101928373
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370

2019
dbSNP: rs3757155
rs3757155
PDE7B
CUI: C0017612
Disease: Glaucoma, Open-Angle
Glaucoma, Open-Angle 		C 0.700 GeneticVariation GWASCAT A multiethnic genome-wide association study of primary open-angle glaucoma identifies novel risk loci. 29891935

2018
dbSNP: rs3799385
rs3799385
PDE7B
CUI: C0410702
Disease: Adolescent idiopathic scoliosis
Adolescent idiopathic scoliosis 		0.700 GeneticVariation GWASCAT The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease. 30019117

2018
dbSNP: rs3799385
rs3799385
PDE7B
CUI: C1837461
Disease: SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3 		0.700 GeneticVariation GWASCAT The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease. 30019117

2018
dbSNP: rs3823159
rs3823159
PDE7B
CUI: C0027404
Disease: Narcolepsy
Narcolepsy 		0.700 GeneticVariation GWASDB Genome-wide association database developed in the Japanese Integrated Database Project. 19629137

2009
dbSNP: rs4896199
rs4896199
PDE7B
CUI: C0040420
Disease: Tonometry
Tonometry 		A 0.700 GeneticVariation GWASCAT Genome-wide association analyses identify new loci influencing intraocular pressure. 29617998

2018
dbSNP: rs761545809
rs761545809
PDE7B
CUI: C0012813
Disease: Diverticulitis
Diverticulitis 		A 0.700 GeneticVariation GWASCAT Sequence variants in ARHGAP15, COLQ and FAM155A associate with diverticular disease and diverticulitis. 28585551

2017
dbSNP: rs78928932
rs78928932
PDE7B ; LOC101928373
CUI: C1314691
Disease: Age at menarche
Age at menarche 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370

2019
dbSNP: rs9494457
rs9494457
PDE7B
CUI: C0040420
Disease: Tonometry
Tonometry 		0.700 GeneticVariation GWASCAT Genome-wide association study of intraocular pressure uncovers new pathways to glaucoma. 30054594

2018
dbSNP: rs9494457
rs9494457
PDE7B
CUI: C0017601
Disease: Glaucoma
Glaucoma 		0.700 GeneticVariation GWASCAT Genome-wide association study of intraocular pressure uncovers new pathways to glaucoma. 30054594

2018
dbSNP: rs9494457
rs9494457
PDE7B
CUI: C0040420
Disease: Tonometry
Tonometry 		T 0.700 GeneticVariation GWASCAT Genome-wide analyses identify 68 new loci associated with intraocular pressure and improve risk prediction for primary open-angle glaucoma. 29785010

2018
dbSNP: rs9494457
rs9494457
PDE7B
CUI: C0040420
Disease: Tonometry
Tonometry 		T 0.700 GeneticVariation GWASCAT Genome-wide association analyses identify new loci influencing intraocular pressure. 29617998

2018