Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs61750434
rs61750434
PEX10
A 0.700 GeneticVariation CLINVAR Phenotype-genotype relationships in PEX10-deficient peroxisome biogenesis disorder patients. 10862081

2000
dbSNP: rs61750434
rs61750434
PEX10
A 0.700 GeneticVariation CLINVAR Identification of PEX10, the gene defective in complementation group 7 of the peroxisome-biogenesis disorders. 9683594

1998