Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs137853058
rs137853058
PRKN
0.020 GeneticVariation BEFREE Steele-Richardson-Olszewski syndrome in a patient with a single C212Y mutation in the parkin protein. 12465088

2002
dbSNP: rs137853058
rs137853058
PRKN
0.020 GeneticVariation BEFREE Progressive supranuclear palsy and tau hyperphosphorylation in a patient with a C212Y parkin mutation. 12446971

2002