rs63750756, MAPT

N. diseases: 23
Disease: Dysautonomia ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Dysautonomia
CUI: C0013363
Disease: Dysautonomia
0.010 GeneticVariation BEFREE Physiologic assessment of autonomic dysfunction in pallidopontonigral degeneration with N279K mutation in the tau gene on chromosome 17. 12492138 2002