rs1555462347, USP7

N. diseases: 34
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Mild Mental Retardation
CUI: C0026106
Disease: Mild Mental Retardation
0.700 GeneticVariation CLINVAR
Hyperpigmentation
CUI: C0162834
Disease: Hyperpigmentation
0.700 GeneticVariation CLINVAR
Overriding toe
CUI: C0920299
Disease: Overriding toe
0.700 GeneticVariation CLINVAR
Few cafe-au-lait spots
CUI: C4024881
Disease: Few cafe-au-lait spots
0.700 GeneticVariation CLINVAR
Gross motor development delay
CUI: C1837658
Disease: Gross motor development delay
0.700 GeneticVariation CLINVAR
Reduced fetal movement
CUI: C0235659
Disease: Reduced fetal movement
0.700 GeneticVariation CLINVAR
Sleep disturbances
CUI: C0037317
Disease: Sleep disturbances
0.700 GeneticVariation CLINVAR
Sleep Apnea Syndromes
CUI: C0037315
Disease: Sleep Apnea Syndromes
0.700 GeneticVariation CLINVAR
Anxiety
CUI: C0003467
Disease: Anxiety
0.700 GeneticVariation CLINVAR
Vesico-Ureteral Reflux
CUI: C0042580
Disease: Vesico-Ureteral Reflux
0.700 GeneticVariation CLINVAR
Abnormal muscle tone
CUI: C0852413
Disease: Abnormal muscle tone
0.700 GeneticVariation CLINVAR
Recurrent urinary tract infection
CUI: C0262655
Disease: Recurrent urinary tract infection
0.700 GeneticVariation CLINVAR
Expressive language delay
CUI: C0454641
Disease: Expressive language delay
0.700 GeneticVariation CLINVAR
Secondary Caesarian section
CUI: C4072904
Disease: Secondary Caesarian section
0.700 GeneticVariation CLINVAR
Complex partial seizure with impairment of consciousness
CUI: C0270834
Disease: Complex partial seizure with impairment of consciousness
0.700 GeneticVariation CLINVAR
Seizures
CUI: C0036572
Disease: Seizures
0.700 GeneticVariation CLINVAR
Macrodontia
CUI: C0266036
Disease: Macrodontia
0.700 GeneticVariation CLINVAR
EEG with generalized slow activity
CUI: C4021217
Disease: EEG with generalized slow activity
0.700 GeneticVariation CLINVAR
Myoclonus
CUI: C0027066
Disease: Myoclonus
0.700 GeneticVariation CLINVAR
Short fourth metatarsal
CUI: C1848514
Disease: Short fourth metatarsal
0.700 GeneticVariation CLINVAR
Fecal Incontinence
CUI: C0015732
Disease: Fecal Incontinence
0.700 GeneticVariation CLINVAR
Abnormal behavior
CUI: C0233514
Disease: Abnormal behavior
0.700 GeneticVariation CLINVAR
Easy fatigability
CUI: C1837098
Disease: Easy fatigability
0.700 GeneticVariation CLINVAR
Short third metatarsal
CUI: C4021650
Disease: Short third metatarsal
0.700 GeneticVariation CLINVAR
Optic Neuropathy
CUI: C3887709
Disease: Optic Neuropathy
0.700 GeneticVariation CLINVAR