RS863225083 PEX6
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What This Variant Does
"CLNSIG=5
Associated Conditions
Heimler syndrome 2
Peroxisome biogenesis disorder 4A (Zellweger)
Peroxisome biogenesis disorder 4B
Peroxisome biogenesis disorder
Inborn genetic diseases
Heimler syndrome 2
Peroxisome biogenesis disorder 4A (Zellweger)
Peroxisome biogenesis disorder 4B
Peroxisome biogenesis disorder
Inborn genetic diseases
Other Variants in PEX6