RS869312935 PEX10

Health Risk Chr 1:2406719
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What This Variant Does
"CLNSIG=5
Associated Conditions
Inborn genetic diseases
Peroxisome biogenesis disorder
complementation group 7
Peroxisome biogenesis disorder
complementation group 7
Peroxisome biogenesis disorder 6A (Zellweger)
Inborn genetic diseases
Peroxisome biogenesis disorder
complementation group 7
Peroxisome biogenesis disorder
complementation group 7
Peroxisome biogenesis disorder 6A (Zellweger)
Other Variants in PEX10
rs267608183 rs61752095 rs61750434 rs61750435 rs724159999 rs724160000 rs724160001 rs724160002 rs61752092 rs61736380
Ask Dr. Hemsworth about this variant