Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs751037529
rs751037529
PRKN
0.010 GeneticVariation BEFREE Heterozygous c.850G>C mutation carriers were free of any neurological symptoms, consistent with a loss-of-function mechanism of the parkin mutations. 27177722

2016