rs867410737, ATP5F1D

N. diseases: 45
Disease: Rhabdomyolysis ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Rhabdomyolysis
CUI: C0035410
Disease: Rhabdomyolysis
0.700 CausalMutation CLINVAR Biallelic Mutations in ATP5F1D, which Encodes a Subunit of ATP Synthase, Cause a Metabolic Disorder. 29478781 2018