rs242557, MAPT

N. diseases: 12
Disease: Parkinsonian Disorders ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Parkinsonian Disorders
CUI: C0242422
Disease: Parkinsonian Disorders
0.010 GeneticVariation BEFREE The rs242557 polymorphism could act modulating the phenotypic expressivity of the H1 risk on these parkinsonisms. 19879020 2011