Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs368134308
rs368134308
Entrez Id: 5071
Gene Symbol: PRKN
PRKN
CUI: C0242422
Disease:
Parkinsonian Disorders
0.010 GeneticVariation BEFREE New mutation (R42P) of the parkin gene in the ubiquitinlike domain associated with parkinsonism. 11222788 2001