ZNF652, zinc finger protein 652, 22834

N. diseases: 37; N. variants: 15
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs7210100
rs7210100
Entrez Id: 22834;102724596
Gene Symbol: ZNF652;LOC102724596
ZNF652;LOC102724596
CUI: C0600139
Disease:
Prostate carcinoma 		0.710 GeneticVariation BEFREE Of the 82 known risk variants, 68 (83%) had effects that were directionally consistent in their association with prostate cancer risk and 30 (37%) were significantly associated with risk at p < 0.05, with the most statistically significant variants being rs116041037 (p = 3.7 × 10(-26) ) and rs6983561 (p = 1.1 × 10(-16) ) at 8q24, as well as rs7210100 (p = 5.4 × 10(-8) ) at 17q21. 25044450 2015
dbSNP: rs7210100
rs7210100
Entrez Id: 22834;102724596
Gene Symbol: ZNF652;LOC102724596
ZNF652;LOC102724596
CUI: C0376358
Disease:
Malignant neoplasm of prostate 		0.710 GeneticVariation BEFREE Of the 82 known risk variants, 68 (83%) had effects that were directionally consistent in their association with prostate cancer risk and 30 (37%) were significantly associated with risk at p < 0.05, with the most statistically significant variants being rs116041037 (p = 3.7 × 10(-26) ) and rs6983561 (p = 1.1 × 10(-16) ) at 8q24, as well as rs7210100 (p = 5.4 × 10(-8) ) at 17q21. 25044450 2015
dbSNP: rs7210100
rs7210100
Entrez Id: 22834;102724596
Gene Symbol: ZNF652;LOC102724596
ZNF652;LOC102724596
CUI: C0600139
Disease:
Prostate carcinoma 		0.710 GeneticVariation GWASCAT Genome-wide association study of prostate cancer in men of African ancestry identifies a susceptibility locus at 17q21. 21602798 2011
dbSNP: rs7210100
rs7210100
Entrez Id: 22834;102724596
Gene Symbol: ZNF652;LOC102724596
ZNF652;LOC102724596
CUI: C0376358
Disease:
Malignant neoplasm of prostate 		0.710 GeneticVariation GWASDB Genome-wide association study of prostate cancer in men of African ancestry identifies a susceptibility locus at 17q21. 21602798 2011
dbSNP: rs112502960
rs112502960
Entrez Id: 22834;102724596
Gene Symbol: ZNF652;LOC102724596
ZNF652;LOC102724596
CUI: C0004096
Disease:
Asthma 		A 0.700 GeneticVariation GWASCAT Moderate-to-severe asthma in individuals of European ancestry: a genome-wide association study. 30552067 2019
dbSNP: rs12185242
rs12185242
Entrez Id: 22834
Gene Symbol: ZNF652
ZNF652
CUI: C0013595
Disease:
Eczema 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs16948048
rs16948048
Entrez Id: 22834;102724596
Gene Symbol: ZNF652;LOC102724596
ZNF652;LOC102724596
CUI: C0005890
Disease:
Body Height 		0.700 GeneticVariation GWASCAT Characterizing rare and low-frequency height-associated variants in the Japanese population. 31562340 2019
dbSNP: rs2072153
rs2072153
Entrez Id: 22834
Gene Symbol: ZNF652
ZNF652
CUI: C1261502
Disease:
Finding of Mean Corpuscular Hemoglobin 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs35587648
rs35587648
Entrez Id: 22834
Gene Symbol: ZNF652
ZNF652
CUI: C0005890
Disease:
Body Height 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs9889262
rs9889262
Entrez Id: 22834
Gene Symbol: ZNF652
ZNF652
CUI: C0035242
Disease:
Respiratory Tract Diseases 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs11652146
rs11652146
Entrez Id: 22834
Gene Symbol: ZNF652
ZNF652
CUI: C0202117
Disease:
Low density lipoprotein cholesterol measurement 		0.700 GeneticVariation GWASCAT Heritability informed power optimization (HIPO) leads to enhanced detection of genetic associations across multiple traits. 30289880 2018
dbSNP: rs11652146
rs11652146
Entrez Id: 22834
Gene Symbol: ZNF652
ZNF652
CUI: C1445957
Disease:
Serum total cholesterol measurement 		0.700 GeneticVariation GWASCAT Heritability informed power optimization (HIPO) leads to enhanced detection of genetic associations across multiple traits. 30289880 2018
dbSNP: rs11652146
rs11652146
Entrez Id: 22834
Gene Symbol: ZNF652
ZNF652
CUI: C0392885
Disease:
High density lipoprotein measurement 		0.700 GeneticVariation GWASCAT Heritability informed power optimization (HIPO) leads to enhanced detection of genetic associations across multiple traits. 30289880 2018
dbSNP: rs11652146
rs11652146
Entrez Id: 22834
Gene Symbol: ZNF652
ZNF652
CUI: C0202236
Disease:
Triglycerides measurement 		0.700 GeneticVariation GWASCAT Heritability informed power optimization (HIPO) leads to enhanced detection of genetic associations across multiple traits. 30289880 2018
dbSNP: rs16948048
rs16948048
Entrez Id: 22834;102724596
Gene Symbol: ZNF652;LOC102724596
ZNF652;LOC102724596
CUI: C1956346
Disease:
Coronary Artery Disease 		A 0.700 GeneticVariation GWASCAT Identification of 64 Novel Genetic Loci Provides an Expanded View on the Genetic Architecture of Coronary Artery Disease. 29212778 2018
dbSNP: rs62076439
rs62076439
Entrez Id: 22834
Gene Symbol: ZNF652
ZNF652
CUI: C1956346
Disease:
Coronary Artery Disease 		T 0.700 GeneticVariation GWASCAT Identification of 64 Novel Genetic Loci Provides an Expanded View on the Genetic Architecture of Coronary Artery Disease. 29212778 2018
dbSNP: rs12940887
rs12940887
Entrez Id: 22834
Gene Symbol: ZNF652
ZNF652
CUI: C0428883
Disease:
Diastolic blood pressure 		T 0.700 GeneticVariation GWASCAT Novel Blood Pressure Locus and Gene Discovery Using Genome-Wide Association Study and Expression Data Sets From Blood and the Kidney. 28739976 2017
dbSNP: rs1343795
rs1343795
Entrez Id: 22834
Gene Symbol: ZNF652
ZNF652
CUI: C0006826
Disease:
Malignant Neoplasms 		A 0.700 GeneticVariation GWASCAT Cancer risk susceptibility loci in a Swedish population. 29299148 2017
dbSNP: rs16948048
rs16948048
Entrez Id: 22834;102724596
Gene Symbol: ZNF652;LOC102724596
ZNF652;LOC102724596
CUI: C0871470
Disease:
Systolic Pressure 		A 0.700 GeneticVariation GWASCAT Genome-wide association analyses using electronic health records identify new loci influencing blood pressure variation. 27841878 2017
dbSNP: rs16948048
rs16948048
Entrez Id: 22834;102724596
Gene Symbol: ZNF652;LOC102724596
ZNF652;LOC102724596
CUI: C0428883
Disease:
Diastolic blood pressure 		A 0.700 GeneticVariation GWASCAT Genome-wide association analyses using electronic health records identify new loci influencing blood pressure variation. 27841878 2017
dbSNP: rs16948048
rs16948048
Entrez Id: 22834;102724596
Gene Symbol: ZNF652;LOC102724596
ZNF652;LOC102724596
CUI: C0006826
Disease:
Malignant Neoplasms 		A 0.700 GeneticVariation GWASCAT Cancer risk susceptibility loci in a Swedish population. 29299148 2017
dbSNP: rs7225787
rs7225787
Entrez Id: 22834
Gene Symbol: ZNF652
ZNF652
CUI: C0006826
Disease:
Malignant Neoplasms 		A 0.700 GeneticVariation GWASCAT Cancer risk susceptibility loci in a Swedish population. 29299148 2017
dbSNP: rs9889262
rs9889262
Entrez Id: 22834
Gene Symbol: ZNF652
ZNF652
CUI: C1527304
Disease:
Allergic Reaction 		A 0.700 GeneticVariation GWASCAT Shared genetic origin of asthma, hay fever and eczema elucidates allergic disease biology. 29083406 2017
dbSNP: rs12940887
rs12940887
Entrez Id: 22834
Gene Symbol: ZNF652
ZNF652
CUI: C0428883
Disease:
Diastolic blood pressure 		T 0.700 GeneticVariation GWASCAT The genetics of blood pressure regulation and its target organs from association studies in 342,415 individuals. 27618452 2016
dbSNP: rs12940887
rs12940887
Entrez Id: 22834
Gene Symbol: ZNF652
ZNF652
CUI: C0871470
Disease:
Systolic Pressure 		T 0.700 GeneticVariation GWASCAT The genetics of blood pressure regulation and its target organs from association studies in 342,415 individuals. 27618452 2016