rs761665644, TYMP;SCO2

N. diseases: 4
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Mitochondrial DNA Depletion Syndrome 1
CUI: C4551995
Disease: Mitochondrial DNA Depletion Syndrome 1
0.700 CausalMutation CLINVAR
Gastrointestinal dysmotility
CUI: C1836923
Disease: Gastrointestinal dysmotility
0.700 CausalMutation CLINVAR
Peripheral Neuropathy
CUI: C0031117
Disease: Peripheral Neuropathy
0.700 CausalMutation CLINVAR
Extraocular Muscle Paresis
CUI: C0262918
Disease: Extraocular Muscle Paresis
0.700 CausalMutation CLINVAR