rs398122414, PRNP

N. diseases: 3
Disease: Prion Diseases ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Prion Diseases
CUI: C0162534
Disease: Prion Diseases
0.010 GeneticVariation BEFREE Familial human prion diseases associated with prion protein mutations Y226X and G131V are transmissible to transgenic mice expressing human prion protein. 29458424 2018