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: 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: 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: rs116890317
rs116890317
Entrez Id: 22834
Gene Symbol: ZNF652
ZNF652
CUI: C0376358
Disease:
Malignant neoplasm of prostate 		0.010 GeneticVariation BEFREE Two ZNF652 (17q21.3) variants, rs116890317 and rs79670217, increased the risk of both sporadic and hereditary PrCa (rs116890317: OR = 3.3-7.8, p = 0.003-3.3 × 10(-5) ; rs79670217: OR = 1.6-1.9, p = 0.002-0.009). 25335771 2015
dbSNP: rs116890317
rs116890317
Entrez Id: 22834
Gene Symbol: ZNF652
ZNF652
CUI: C0600139
Disease:
Prostate carcinoma 		0.010 GeneticVariation BEFREE Two ZNF652 (17q21.3) variants, rs116890317 and rs79670217, increased the risk of both sporadic and hereditary PrCa (rs116890317: OR = 3.3-7.8, p = 0.003-3.3 × 10(-5) ; rs79670217: OR = 1.6-1.9, p = 0.002-0.009). 25335771 2015
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: 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: rs12940887
rs12940887
Entrez Id: 22834
Gene Symbol: ZNF652
ZNF652
CUI: C1306620
Disease:
Systolic blood pressure measurement 		0.700 GeneticVariation GWASDB Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk. 21909115 2011
dbSNP: rs12940887
rs12940887
Entrez Id: 22834
Gene Symbol: ZNF652
ZNF652
CUI: C0005823
Disease:
Blood Pressure 		T 0.700 GeneticVariation GWASDB Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure. 21909110 2011
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
dbSNP: rs12940887
rs12940887
Entrez Id: 22834
Gene Symbol: ZNF652
ZNF652
CUI: C0428886
Disease:
Mean blood pressure 		T 0.700 GeneticVariation GWASCAT Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure. 21909110 2011
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: rs1343795
rs1343795
Entrez Id: 22834
Gene Symbol: ZNF652
ZNF652
CUI: C0011615
Disease:
Dermatitis, Atopic 		0.010 GeneticVariation BEFREE We also identified 3 suggestive (P < 5×10) loci with maternal genetic effects: 1 for any FA (rs976078, in a gene desert region on 13q31.1) and 2 for egg allergy (rs1343795 and rs4572450, in the ZNF652 gene, where genetic variants have been associated with atopic dermatitis). 29489655 2018
dbSNP: rs1343795
rs1343795
Entrez Id: 22834
Gene Symbol: ZNF652
ZNF652
CUI: C0013595
Disease:
Eczema 		0.010 GeneticVariation BEFREE We also identified 3 suggestive (P < 5×10) loci with maternal genetic effects: 1 for any FA (rs976078, in a gene desert region on 13q31.1) and 2 for egg allergy (rs1343795 and rs4572450, in the ZNF652 gene, where genetic variants have been associated with atopic dermatitis). 29489655 2018
dbSNP: rs1343795
rs1343795
Entrez Id: 22834
Gene Symbol: ZNF652
ZNF652
CUI: C0559469
Disease:
Allergy to eggs 		0.010 GeneticVariation BEFREE We also identified 3 suggestive (P < 5×10) loci with maternal genetic effects: 1 for any FA (rs976078, in a gene desert region on 13q31.1) and 2 for egg allergy (rs1343795 and rs4572450, in the ZNF652 gene, where genetic variants have been associated with atopic dermatitis). 29489655 2018
dbSNP: rs1343795
rs1343795
Entrez Id: 22834
Gene Symbol: ZNF652
ZNF652
CUI: C4554344
Disease:
IgE-mediated food allergy 		0.010 GeneticVariation BEFREE We also identified 3 suggestive (P < 5×10) loci with maternal genetic effects: 1 for any FA (rs976078, in a gene desert region on 13q31.1) and 2 for egg allergy (rs1343795 and rs4572450, in the ZNF652 gene, where genetic variants have been associated with atopic dermatitis). 29489655 2018
dbSNP: rs16948048
rs16948048
Entrez Id: 22834;102724596
Gene Symbol: ZNF652;LOC102724596
ZNF652;LOC102724596
CUI: C1305849
Disease:
Diastolic blood pressure measurement 		G 0.700 GeneticVariation GWASDB Genome-wide association study identifies eight loci associated with blood pressure. 19430483 2009
dbSNP: rs16948048
rs16948048
Entrez Id: 22834;102724596
Gene Symbol: ZNF652;LOC102724596
ZNF652;LOC102724596
CUI: C0428883
Disease:
Diastolic blood pressure 		A 0.700 GeneticVariation GWASCAT Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension. 27618447 2016
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: C0005823
Disease:
Blood Pressure 		0.700 GeneticVariation GWASDB Association of genetic variation with systolic and diastolic blood pressure among African Americans: the Candidate Gene Association Resource study. 21378095 2011
dbSNP: rs16948048
rs16948048
Entrez Id: 22834;102724596
Gene Symbol: ZNF652;LOC102724596
ZNF652;LOC102724596
CUI: C0428883
Disease:
Diastolic blood pressure 		G 0.700 GeneticVariation GWASCAT Genome-wide association study identifies eight loci associated with blood pressure. 19430483 2009
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