Gene: TREM2 ×
Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs753325601
rs753325601
TREM2 ; LOC105375056
0.010 GeneticVariation BEFREE Targeted exome sequencing reveals homozygous TREM2 R47C mutation presenting with behavioral variant frontotemporal dementia without bone involvement. 29748150

2018