rs74315401, PRNP

N. diseases: 32
Disease: Familial (FPAH) ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Familial (FPAH)
CUI: C1611743
Disease: Familial (FPAH)
0.010 GeneticVariation BEFREE This line of mice was generated to model the mutation thought to be responsible for P102L GSS, a familial TSE disease in humans. 12733430 2003