RS863225084 PEX1
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=5
Associated Conditions
Heimler syndrome 1
Retinal dystrophy
Peroxisome biogenesis disorder 1A (Zellweger)
Peroxisome biogenesis disorder 1B
Zellweger spectrum disorders
PEX1-related disorder
Heimler syndrome 1
Retinal dystrophy
Peroxisome biogenesis disorder 1A (Zellweger)
Peroxisome biogenesis disorder 1B
Zellweger spectrum disorders
PEX1-related disorder
Other Variants in PEX1