RS145888212 PEX14

Health Risk Chr 1:10623085
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Associated Conditions
Inborn genetic diseases
Peroxisome biogenesis disorder
complementation group K
Inborn genetic diseases
Peroxisome biogenesis disorder
complementation group K
Other Variants in PEX14
rs61752116 rs146359055 rs148479162 rs727504081 rs147706488 rs200154696 rs145867351 rs41274484 rs143412169 rs112851814
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