GRN, granulin precursor, 2896

N. diseases: 412; N. variants: 66
Disease: Primary Progressive Aphasia (disorder) ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs764232836
rs764232836
Entrez Id: 2896
Gene Symbol: GRN
GRN
CUI: C0282513
Disease:
Primary Progressive Aphasia (disorder) 		0.010 GeneticVariation BEFREE Rare risk variants, TREM2 R47H and MAPT A152T, were associated with a three- to seven-fold increase in risk for PPA. 30599136 2019