RS764791523 SPG7

Health Risk Chr 16:89526389
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What This Variant Does
"CLNSIG=5
Associated Conditions
Hereditary spastic paraplegia 7
Inborn genetic diseases
Optic atrophy
Hereditary spastic paraplegia 7
Inborn genetic diseases
Optic atrophy
Other Variants in SPG7
rs1597661607 rs121918357 rs121918358 rs141659620 rs267607085 rs61755320 rs116319889 rs202070075 rs111475461 rs574656941
Ask Dr. Hemsworth about this variant