rs63751273, MAPT

N. diseases: 42
Disease: Motor symptoms ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Motor symptoms
CUI: C0426980
Disease: Motor symptoms
0.010 GeneticVariation BEFREE We also examined postural sway in mice expressing mutations that mimic frontotemporal dementia with Parkinsonism linked to chromosome 17 (FTDP-17) (T-279, P301L or P301L-nitric oxide synthase 2 (NOS2)(-/-) mice) and that demonstrate motor symptoms. 17764851 2007