Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs104893878
rs104893878
0.020 GeneticVariation BEFREE Familial parkinsonism with synuclein pathology: clinical and PET studies of A30P mutation carriers. 11376188

2001

dbSNP: rs104893878
rs104893878
0.020 GeneticVariation BEFREE Six α-synuclein (aSyn) point mutations are currently known to be associated with familial parkinsonism: A30P, E46K, H50Q, G51D, A53E, and A53T. 30605594

2019