RS749067142 PEX1

Health Risk Chr 7:92517732
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What This Variant Does
"CLNSIG=4
Associated Conditions
Peroxisome biogenesis disorder 1A (Zellweger)
Peroxisome biogenesis disorder 1B
Zellweger spectrum disorders
Peroxisome biogenesis disorder
Inborn genetic diseases
Heimler syndrome 1
PEX1-related disorder
Peroxisome biogenesis disorder 1A (Zellweger)
Peroxisome biogenesis disorder 1B
Zellweger spectrum disorders
Peroxisome biogenesis disorder
Inborn genetic diseases
Heimler syndrome 1
PEX1-related disorder
Other Variants in PEX1
rs61750420 rs121434455 rs1554372074 rs61750415 rs398123408 rs398123409 rs145430946 rs144825021 rs71560821 rs372485912
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