Gene: PRKN ×
Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs199657839
rs199657839
PRKN
0.010 GeneticVariation BEFREE These include five missense mutations (Gln34Arg, Arg42Cys, Arg42His, Tyr143Cys and Arg334Cys) detected in eight patients in heterozygous condition and a homozygous deletion encompassing exons 3 and 4 in two sibs affected with PD. 16793319

2006
dbSNP: rs368134308
rs368134308
PRKN
0.010 GeneticVariation BEFREE These include five missense mutations (Gln34Arg, Arg42Cys, Arg42His, Tyr143Cys and Arg334Cys) detected in eight patients in heterozygous condition and a homozygous deletion encompassing exons 3 and 4 in two sibs affected with PD. 16793319

2006
dbSNP: rs778798543
rs778798543
PRKN
0.010 GeneticVariation BEFREE These include five missense mutations (Gln34Arg, Arg42Cys, Arg42His, Tyr143Cys and Arg334Cys) detected in eight patients in heterozygous condition and a homozygous deletion encompassing exons 3 and 4 in two sibs affected with PD. 16793319

2006
dbSNP: rs1258359845
rs1258359845
PRKN
0.010 GeneticVariation BEFREE In order to analyse the association of PD with these and two previously described polymorphisms (1281 G/A, Asp394Asn, and 601 G/A, Ser167Asn) we genotyped 105 patients and 150 healthy controls. 12165399

2002
dbSNP: rs56092260
rs56092260
PRKN
0.010 GeneticVariation BEFREE A polymorphism of R/W366 in the Parkin gene was found to be associated with a protective factor for sporadic PD. 10965160

2000