RS138843050 PEX10

Health Risk Chr 1:2408627
Upload your DNA to see your genotype for this variant.
Associated Conditions
Peroxisome biogenesis disorder
complementation group 7
Zellweger spectrum disorders
Inborn genetic diseases
Peroxisome biogenesis disorder
complementation group 7
Zellweger spectrum disorders
Inborn genetic diseases
Other Variants in PEX10
rs267608183 rs61752095 rs61750434 rs61750435 rs724159999 rs724160000 rs724160001 rs724160002 rs61752092 rs61736380
Ask Dr. Hemsworth about this variant