RS398123301 PEX12

Health Risk Chr 17:35575973
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What This Variant Does
"CLNSIG=5
Associated Conditions
Peroxisome biogenesis disorder 3A (Zellweger)
Peroxisome biogenesis disorder type 3B
Peroxisome biogenesis disorder
Inborn genetic diseases
PEX12-related disorder
Peroxisome biogenesis disorder 3A (Zellweger)
Peroxisome biogenesis disorder type 3B
Peroxisome biogenesis disorder
Inborn genetic diseases
PEX12-related disorder
Other Variants in PEX12
rs104894616 rs61752103 rs28936697 rs61752097 rs28936698 rs61752112 rs138731505 rs398123302 rs786205502 rs776731688
Ask Dr. Hemsworth about this variant