RS1060499768 SPG11

Health Risk Chr 15:44584504
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What This Variant Does
"CLNSIG=4
Associated Conditions
Abnormal brain morphology
Hereditary spastic paraplegia 11
Hereditary spastic paraplegia 11
Abnormal brain morphology
Hereditary spastic paraplegia 11
Hereditary spastic paraplegia 11
Other Variants in SPG11
rs118203963 rs312262716 rs267607084 rs312262720 rs312262744 rs312262715 rs200079802 rs141848292 rs312262752 rs312262722
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