Source: ALL

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs63751438
rs63751438
MAPT
CUI: C0393570
Disease: Corticobasal degeneration
Corticobasal degeneration 		0.010 GeneticVariation BEFREE Frontotemporal dementia and corticobasal degeneration in a family with a P301S mutation in tau. 10374757

1999