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: C0042024
Disease: Urinary Incontinence
Urinary Incontinence 		G 0.700 GeneticVariation CLINVAR

dbSNP: rs1555462347
rs1555462347
USP7
CUI: C1848514
Disease: Short fourth metatarsal
Short fourth metatarsal 		G 0.700 GeneticVariation CLINVAR

dbSNP: rs1555462347
rs1555462347
USP7
CUI: C0162834
Disease: Hyperpigmentation
Hyperpigmentation 		G 0.700 GeneticVariation CLINVAR

dbSNP: rs1555462347
rs1555462347
USP7
CUI: C0026106
Disease: Mild Mental Retardation
Mild Mental Retardation 		G 0.700 GeneticVariation CLINVAR

dbSNP: rs1555462347
rs1555462347
USP7
CUI: C4023802
Disease: Hyperextensibility of the knee
Hyperextensibility of the knee 		G 0.700 GeneticVariation CLINVAR

dbSNP: rs1555462347
rs1555462347
USP7
CUI: C1837098
Disease: Easy fatigability
Easy fatigability 		G 0.700 GeneticVariation CLINVAR

dbSNP: rs1555462347
rs1555462347
USP7
CUI: C3887709
Disease: Optic Neuropathy
Optic Neuropathy 		G 0.700 GeneticVariation CLINVAR

dbSNP: rs1555462347
rs1555462347
USP7
CUI: C0003467
Disease: Anxiety
Anxiety 		G 0.700 GeneticVariation CLINVAR

dbSNP: rs1555462347
rs1555462347
USP7
CUI: C0235659
Disease: Reduced fetal movement
Reduced fetal movement 		G 0.700 GeneticVariation CLINVAR

dbSNP: rs1555462347
rs1555462347
USP7
CUI: C0549629
Disease: Abnormal delivery
Abnormal delivery 		G 0.700 GeneticVariation CLINVAR

dbSNP: rs1555462347
rs1555462347
USP7
CUI: C0037317
Disease: Sleep disturbances
Sleep disturbances 		G 0.700 GeneticVariation CLINVAR

dbSNP: rs1555462347
rs1555462347
USP7
CUI: C1837658
Disease: Gross motor development delay
Gross motor development delay 		G 0.700 GeneticVariation CLINVAR

dbSNP: rs1555462347
rs1555462347
USP7
CUI: C0262655
Disease: Recurrent urinary tract infection
Recurrent urinary tract infection 		G 0.700 GeneticVariation CLINVAR

dbSNP: rs1555462347
rs1555462347
USP7
CUI: C4024881
Disease: Few cafe-au-lait spots
Few cafe-au-lait spots 		G 0.700 GeneticVariation CLINVAR

dbSNP: rs1555462347
rs1555462347
USP7
CUI: C0454641
Disease: Expressive language delay
Expressive language delay 		G 0.700 GeneticVariation CLINVAR

dbSNP: rs1555462347
rs1555462347
USP7
CUI: C0042580
Disease: Vesico-Ureteral Reflux
Vesico-Ureteral Reflux 		G 0.700 GeneticVariation CLINVAR

dbSNP: rs1555462347
rs1555462347
USP7
CUI: C4021217
Disease: EEG with generalized slow activity
EEG with generalized slow activity 		G 0.700 GeneticVariation CLINVAR

dbSNP: rs1555462347
rs1555462347
USP7
CUI: C0038379
Disease: Strabismus
Strabismus 		G 0.700 GeneticVariation CLINVAR

dbSNP: rs1555462347
rs1555462347
USP7
CUI: C4072904
Disease: Secondary Caesarian section
Secondary Caesarian section 		G 0.700 GeneticVariation CLINVAR

dbSNP: rs1555462347
rs1555462347
USP7
CUI: C0036572
Disease: Seizures
Seizures 		G 0.700 GeneticVariation CLINVAR

dbSNP: rs1555462347
rs1555462347
USP7
CUI: C0015732
Disease: Fecal Incontinence
Fecal Incontinence 		G 0.700 GeneticVariation CLINVAR

dbSNP: rs1555462347
rs1555462347
USP7
CUI: C0233514
Disease: Abnormal behavior
Abnormal behavior 		G 0.700 GeneticVariation CLINVAR

dbSNP: rs1555462347
rs1555462347
USP7
CUI: C4021649
Disease: Short fifth metatarsal
Short fifth metatarsal 		G 0.700 GeneticVariation CLINVAR

dbSNP: rs1555462347
rs1555462347
USP7
CUI: C0009806
Disease: Constipation
Constipation 		G 0.700 GeneticVariation CLINVAR

dbSNP: rs1555462347
rs1555462347
USP7
CUI: C0266036
Disease: Macrodontia
Macrodontia 		G 0.700 GeneticVariation CLINVAR