Source: ALL

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs149622783
rs149622783
TREM2 ; TREML1 ; LOC105375056
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease 		0.010 GeneticVariation BEFREE In addition, we identified rare variant R136Q in a patient with language-predominant AD that also showed impaired surface expression. 27589997

2016