rs752169833, CHCHD2

N. diseases: 3
Disease: PARKINSON DISEASE 22, AUTOSOMAL DOMINANT ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
PARKINSON DISEASE 22, AUTOSOMAL DOMINANT
CUI: C4225238
Disease: PARKINSON DISEASE 22, AUTOSOMAL DOMINANT
0.800 GeneticVariation UNIPROT CHCHD2 mutations in autosomal dominant late-onset Parkinson's disease: a genome-wide linkage and sequencing study. 25662902 2015
PARKINSON DISEASE 22, AUTOSOMAL DOMINANT
CUI: C4225238
Disease: PARKINSON DISEASE 22, AUTOSOMAL DOMINANT
0.800 CausalMutation CLINVAR