USP7, ubiquitin specific peptidase 7, 7874

N. diseases: 153; N. variants: 7
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs111792818
rs111792818
Entrez Id: 7874;105371074
Gene Symbol: USP7;LOC105371074
USP7;LOC105371074
CUI: C0023508
Disease:
White Blood Cell Count procedure 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs141361914
rs141361914
Entrez Id: 7874
Gene Symbol: USP7
USP7
CUI: C0200638
Disease:
Eosinophil count procedure 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs166232
rs166232
Entrez Id: 7874
Gene Symbol: USP7
USP7
CUI: C0005890
Disease:
Body Height 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs1529916
rs1529916
Entrez Id: 7874
Gene Symbol: USP7
USP7
CUI: C0024623
Disease:
Malignant neoplasm of stomach 		0.010 GeneticVariation BEFREE We found that the polymorphisms of P53 (rs1042522) and MDM2 (rs2279744) are associated with gastric cancer risk, whereas no significant association was observed between variant genotype of other two polymorphisms (MDM4 rs1380576 and Hausp rs1529916) and gastric cancer risk. 25479941 2015
dbSNP: rs1529916
rs1529916
Entrez Id: 7874
Gene Symbol: USP7
USP7
CUI: C0699791
Disease:
Stomach Carcinoma 		0.010 GeneticVariation BEFREE We found that the polymorphisms of P53 (rs1042522) and MDM2 (rs2279744) are associated with gastric cancer risk, whereas no significant association was observed between variant genotype of other two polymorphisms (MDM4 rs1380576 and Hausp rs1529916) and gastric cancer risk. 25479941 2015
dbSNP: rs1529916
rs1529916
Entrez Id: 7874
Gene Symbol: USP7
USP7
CUI: C0600139
Disease:
Prostate carcinoma 		0.010 GeneticVariation BEFREE Both the Mdm4 and Hausp SNPs (rs1380576 and rs1529916) were found to be associated with higher D'Amico risk prostate cancer category at the time of diagnosis (P = 0.023 and P = 0.046, respectively). 20855462 2010
dbSNP: rs1529916
rs1529916
Entrez Id: 7874
Gene Symbol: USP7
USP7
CUI: C0376358
Disease:
Malignant neoplasm of prostate 		0.010 GeneticVariation BEFREE Both the Mdm4 and Hausp SNPs (rs1380576 and rs1529916) were found to be associated with higher D'Amico risk prostate cancer category at the time of diagnosis (P = 0.023 and P = 0.046, respectively). 20855462 2010
dbSNP: rs7190551
rs7190551
Entrez Id: 7874
Gene Symbol: USP7
USP7
CUI: C3828530
Disease:
Platelet Component Distribution Width Measurement 		A 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs183725
rs183725
Entrez Id: 7874
Gene Symbol: USP7
USP7
CUI: C0032181
Disease:
Platelet Count measurement 		C 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs1555462347
rs1555462347
Entrez Id: 7874
Gene Symbol: USP7
USP7
CUI: C0026106
Disease:
Mild Mental Retardation 		G 0.700 GeneticVariation CLINVAR
dbSNP: rs1555462347
rs1555462347
Entrez Id: 7874
Gene Symbol: USP7
USP7
CUI: C0162834
Disease:
Hyperpigmentation 		G 0.700 GeneticVariation CLINVAR
dbSNP: rs1555462347
rs1555462347
Entrez Id: 7874
Gene Symbol: USP7
USP7
CUI: C0920299
Disease:
Overriding toe 		G 0.700 GeneticVariation CLINVAR
dbSNP: rs1555462347
rs1555462347
Entrez Id: 7874
Gene Symbol: USP7
USP7
CUI: C4024881
Disease:
Few cafe-au-lait spots 		G 0.700 GeneticVariation CLINVAR
dbSNP: rs1555462347
rs1555462347
Entrez Id: 7874
Gene Symbol: USP7
USP7
CUI: C1837658
Disease:
Gross motor development delay 		G 0.700 GeneticVariation CLINVAR
dbSNP: rs1555462347
rs1555462347
Entrez Id: 7874
Gene Symbol: USP7
USP7
CUI: C0235659
Disease:
Reduced fetal movement 		G 0.700 GeneticVariation CLINVAR
dbSNP: rs1555462347
rs1555462347
Entrez Id: 7874
Gene Symbol: USP7
USP7
CUI: C0037317
Disease:
Sleep disturbances 		G 0.700 GeneticVariation CLINVAR
dbSNP: rs1555462347
rs1555462347
Entrez Id: 7874
Gene Symbol: USP7
USP7
CUI: C0037315
Disease:
Sleep Apnea Syndromes 		G 0.700 GeneticVariation CLINVAR
dbSNP: rs1555462347
rs1555462347
Entrez Id: 7874
Gene Symbol: USP7
USP7
CUI: C0003467
Disease:
Anxiety 		G 0.700 GeneticVariation CLINVAR
dbSNP: rs1555462347
rs1555462347
Entrez Id: 7874
Gene Symbol: USP7
USP7
CUI: C0042580
Disease:
Vesico-Ureteral Reflux 		G 0.700 GeneticVariation CLINVAR
dbSNP: rs1555462347
rs1555462347
Entrez Id: 7874
Gene Symbol: USP7
USP7
CUI: C0852413
Disease:
Abnormal muscle tone 		G 0.700 GeneticVariation CLINVAR
dbSNP: rs1555462347
rs1555462347
Entrez Id: 7874
Gene Symbol: USP7
USP7
CUI: C0262655
Disease:
Recurrent urinary tract infection 		G 0.700 GeneticVariation CLINVAR
dbSNP: rs1555462347
rs1555462347
Entrez Id: 7874
Gene Symbol: USP7
USP7
CUI: C0454641
Disease:
Expressive language delay 		G 0.700 GeneticVariation CLINVAR
dbSNP: rs1555462347
rs1555462347
Entrez Id: 7874
Gene Symbol: USP7
USP7
CUI: C4072904
Disease:
Secondary Caesarian section 		G 0.700 GeneticVariation CLINVAR
dbSNP: rs1555462347
rs1555462347
Entrez Id: 7874
Gene Symbol: USP7
USP7
CUI: C0270834
Disease:
Complex partial seizure with impairment of consciousness 		G 0.700 GeneticVariation CLINVAR
dbSNP: rs1555462347
rs1555462347
Entrez Id: 7874
Gene Symbol: USP7
USP7
CUI: C0036572
Disease:
Seizures 		G 0.700 GeneticVariation CLINVAR