rs63751273, MAPT

N. diseases: 42
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Hemispatial Neglect
CUI: C0751421
Disease: Hemispatial Neglect
0.010 GeneticVariation BEFREE New features included hemispatial neglect and unilateral resting tremor not previously reported for P301L MAPT mutation. 20561037 2011