RS61750415 PEX1

Health Risk Chr 7:92503169
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What This Variant Does
"CLNSIG=5
Associated Conditions
Peroxisome biogenesis disorder 1A (Zellweger)
Heimler syndrome 1
Peroxisome biogenesis disorder
Peroxisome biogenesis disorder 1B
Zellweger spectrum disorders
Retinal dystrophy
Inborn genetic diseases
PEX1-related disorder
Optic atrophy
Peroxisome biogenesis disorder 1A (Zellweger)
Heimler syndrome 1
Peroxisome biogenesis disorder
Peroxisome biogenesis disorder 1B
Zellweger spectrum disorders
Retinal dystrophy
Other Variants in PEX1
rs61750420 rs121434455 rs1554372074 rs398123408 rs398123409 rs145430946 rs144825021 rs71560821 rs372485912 rs727504076
Ask Dr. Hemsworth about this variant