rs1555462347, USP7

N. diseases: 34
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Multifocal epileptiform discharges
CUI: C4021219
Disease: Multifocal epileptiform discharges
0.700 GeneticVariation CLINVAR
Short fifth metatarsal
CUI: C4021649
Disease: Short fifth metatarsal
0.700 GeneticVariation CLINVAR
Hyperextensibility of the knee
CUI: C4023802
Disease: Hyperextensibility of the knee
0.700 GeneticVariation CLINVAR
Strabismus
CUI: C0038379
Disease: Strabismus
0.700 GeneticVariation CLINVAR
Urinary Incontinence
CUI: C0042024
Disease: Urinary Incontinence
0.700 GeneticVariation CLINVAR
Constipation
CUI: C0009806
Disease: Constipation
0.700 GeneticVariation CLINVAR
Abnormal delivery
CUI: C0549629
Disease: Abnormal delivery
0.700 GeneticVariation CLINVAR
Hypesthesia
CUI: C0020580
Disease: Hypesthesia
0.700 GeneticVariation CLINVAR
Autonomic bladder dysfunction
CUI: C4025212
Disease: Autonomic bladder dysfunction
0.700 GeneticVariation CLINVAR