Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs752169833
rs752169833
CHCHD2
0.800 GeneticVariation UNIPROT CHCHD2 mutations in autosomal dominant late-onset Parkinson's disease: a genome-wide linkage and sequencing study. 25662902

2015
dbSNP: rs864309650
rs864309650
CHCHD2
0.800 GeneticVariation UNIPROT CHCHD2 mutations in autosomal dominant late-onset Parkinson's disease: a genome-wide linkage and sequencing study. 25662902

2015
dbSNP: rs752169833
rs752169833
CHCHD2
T 0.800 CausalMutation CLINVAR

dbSNP: rs864309650
rs864309650
CHCHD2
A 0.800 CausalMutation CLINVAR

dbSNP: rs750014782
rs750014782
CHCHD2
T 0.700 CausalMutation CLINVAR