Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs766251466
rs766251466
C 0.700 CausalMutation CLINVAR Genotypic and phenotypic spectrum of PANK2 mutations in patients with neurodegeneration with brain iron accumulation. 16437574

2006

dbSNP: rs766251466
rs766251466
C 0.700 CausalMutation CLINVAR A novel 3-bp deletion in the PANK2 gene of Dutch patients with pantothenate kinase-associated neurodegeneration: evidence for a founder effect. 16240131

2005