Gene: PRKN ×
Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs369634041
rs369634041
PRKN
0.010 GeneticVariation BEFREE The clinical phenotype comprised of asymmetrical onset, slowly progressive Parkinsonism with levodopa induced motor restlessness in a patient with the novel mutation (c.313 A > T, p. Ile105Phe) while subjects with c.293 G > A, p.Arg98Gln had early onset levodopa responsive symmetrical Parkinsonism. 27592010

2016
dbSNP: rs368134308
rs368134308
PRKN
0.010 GeneticVariation BEFREE New mutation (R42P) of the parkin gene in the ubiquitinlike domain associated with parkinsonism. 11222788

2001