rs760073870, CAPN2

N. diseases: 1
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Tauopathies
CUI: C0949664
Disease: Tauopathies
0.010 GeneticVariation BEFREE P301L tauopathy: confocal immunofluorescence study of perinuclear aggregation of the mutated protein. 12127682 2002