RS767903764 PEX7
Upload your DNA to see your genotype for this variant.
Associated Conditions
Peroxisome biogenesis disorder 9B
Rhizomelic chondrodysplasia punctata type 1
Inborn genetic diseases
Peroxisome biogenesis disorder 9B
Rhizomelic chondrodysplasia punctata type 1
Inborn genetic diseases
Other Variants in PEX7