Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs75932628
rs75932628
Entrez Id: 54209;105375056
Gene Symbol: TREM2;LOC105375056
TREM2;LOC105375056
CUI: C0270736
Disease:
Essential Tremor
0.010 GeneticVariation BEFREE However, taking into account the very low frequency of p.R47H, further confirmatory analyses of larger ET series are needed. 25585992 2015