Source: ALL

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1281129992
rs1281129992
APP
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease 		0.010 GeneticVariation BEFREE The M139V mutation can lead to atypical AD, and genetic background may have a role in determining the phenotype of genetically defined AD. 12810495

2003