Gene: PEX10 ×
Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs61750435
rs61750435
PEX10
CT 0.700 CausalMutation CLINVAR Genetic classification and mutational spectrum of more than 600 patients with a Zellweger syndrome spectrum disorder. 21031596

2011
dbSNP: rs61752093
rs61752093
PEX10
C 0.700 CausalMutation CLINVAR Genetic classification and mutational spectrum of more than 600 patients with a Zellweger syndrome spectrum disorder. 21031596

2011
dbSNP: rs61750435
rs61750435
PEX10
CT 0.700 CausalMutation CLINVAR Zellweger syndrome resulting from maternal isodisomy of chromosome 1. 17702006

2007
dbSNP: rs61752093
rs61752093
PEX10
C 0.700 CausalMutation CLINVAR Genetic heterogeneity of peroxisome biogenesis disorders among Japanese patients: evidence for a founder haplotype for the most common PEX10 gene mutation. 12794690

2003
dbSNP: rs61750435
rs61750435
PEX10
CT 0.700 CausalMutation CLINVAR Phenotype-genotype relationships in PEX10-deficient peroxisome biogenesis disorder patients. 10862081

2000
dbSNP: rs61752093
rs61752093
PEX10
C 0.700 CausalMutation CLINVAR Phenotype-genotype relationships in PEX10-deficient peroxisome biogenesis disorder patients. 10862081

2000