rs201892814, CAPN3

N. diseases: 8
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Progressive spinal muscular atrophy
CUI: C4082951
Disease: Progressive spinal muscular atrophy
0.700 CausalMutation CLINVAR
Absent muscle fiber calpain-3
CUI: C4022625
Disease: Absent muscle fiber calpain-3
0.700 CausalMutation CLINVAR
Romberg's sign positive
CUI: C0240914
Disease: Romberg's sign positive
0.700 CausalMutation CLINVAR
Difficulty walking
CUI: C0311394
Disease: Difficulty walking
0.700 CausalMutation CLINVAR
MIGRAINE WITH OR WITHOUT AURA, SUSCEPTIBILITY TO, 1
CUI: C3887485
Disease: MIGRAINE WITH OR WITHOUT AURA, SUSCEPTIBILITY TO, 1
0.700 CausalMutation CLINVAR
EMG: neuropathic changes
CUI: C4021727
Disease: EMG: neuropathic changes
0.700 CausalMutation CLINVAR
Creatine phosphokinase serum increased
CUI: C0241005
Disease: Creatine phosphokinase serum increased
0.700 CausalMutation CLINVAR
Paresthesia
CUI: C0030554
Disease: Paresthesia
0.700 CausalMutation CLINVAR