Source: ALL

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1373863123
rs1373863123
ACTB
CUI: C0030552
Disease: Paresis
Paresis 		0.010 GeneticVariation BEFREE These phenomena underlie the toxicity of H40Y and may be considered as important triggering factors for the contractile dysfunction, muscle weakness and disease phenotype seen in patients. 27112274

2016