Source: CLINVAR

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1555462347
rs1555462347
USP7
CUI: C0020580
Disease: Hypesthesia
Hypesthesia 		G 0.700 GeneticVariation CLINVAR

dbSNP: rs1555462347
rs1555462347
USP7
CUI: C4021650
Disease: Short third metatarsal
Short third metatarsal 		G 0.700 GeneticVariation CLINVAR

dbSNP: rs1555462347
rs1555462347
USP7
CUI: C0027066
Disease: Myoclonus
Myoclonus 		G 0.700 GeneticVariation CLINVAR

dbSNP: rs1555462347
rs1555462347
USP7
CUI: C0037315
Disease: Sleep Apnea Syndromes
Sleep Apnea Syndromes 		G 0.700 GeneticVariation CLINVAR

dbSNP: rs1555462347
rs1555462347
USP7
CUI: C4025212
Disease: Autonomic bladder dysfunction
Autonomic bladder dysfunction 		G 0.700 GeneticVariation CLINVAR

dbSNP: rs1555462347
rs1555462347
USP7
CUI: C0270834
Disease: Complex partial seizure with impairment of consciousness
Complex partial seizure with impairment of consciousness 		G 0.700 GeneticVariation CLINVAR

dbSNP: rs1555462347
rs1555462347
USP7
CUI: C0852413
Disease: Abnormal muscle tone
Abnormal muscle tone 		G 0.700 GeneticVariation CLINVAR

dbSNP: rs1555462347
rs1555462347
USP7
CUI: C4021219
Disease: Multifocal epileptiform discharges
Multifocal epileptiform discharges 		G 0.700 GeneticVariation CLINVAR

dbSNP: rs1555462347
rs1555462347
USP7
CUI: C0920299
Disease: Overriding toe
Overriding toe 		G 0.700 GeneticVariation CLINVAR