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: 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: 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: 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
dbSNP: rs1555462347
rs1555462347
Entrez Id: 7874
Gene Symbol: USP7
USP7
CUI: C0266036
Disease:
Macrodontia 		G 0.700 GeneticVariation CLINVAR
dbSNP: rs1555462347
rs1555462347
Entrez Id: 7874
Gene Symbol: USP7
USP7
CUI: C4021217
Disease:
EEG with generalized slow activity 		G 0.700 GeneticVariation CLINVAR
dbSNP: rs1555462347
rs1555462347
Entrez Id: 7874
Gene Symbol: USP7
USP7
CUI: C0027066
Disease:
Myoclonus 		G 0.700 GeneticVariation CLINVAR
dbSNP: rs1555462347
rs1555462347
Entrez Id: 7874
Gene Symbol: USP7
USP7
CUI: C1848514
Disease:
Short fourth metatarsal 		G 0.700 GeneticVariation CLINVAR