rs1800014, PRNP

N. diseases: 11
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Abnormal behavior
CUI: C0233514
Disease: Abnormal behavior
0.010 GeneticVariation BEFREE Rare E196K mutation in the PRNP gene of a patient exhibiting behavioral abnormalities. 20005032 2010