Gene: MAPT ×
Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1456103222
rs1456103222
MAPT
0.020 GeneticVariation BEFREE Unusual presentations in patients with E200K familial Creutzfeldt-Jakob disease. 26806765

2016
dbSNP: rs1456103222
rs1456103222
MAPT
0.020 GeneticVariation BEFREE In conclusion, we report unique pathological sleep patterns in early fCJD associated with the E200K mutation. 27251902

2016
dbSNP: rs1378923121
rs1378923121
MAPT
0.010 GeneticVariation BEFREE Familial Creutzfeldt-Jakob disease with a V180I mutation: comparative analysis with pathological findings and diffusion-weighted images. 20051687

2009