RS369223258 TWNK

Health Risk Chr 10:100993505
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Associated Conditions
Infantile onset spinocerebellar ataxia
Hereditary spastic paraplegia
Inborn genetic diseases
Infantile onset spinocerebellar ataxia
Hereditary spastic paraplegia
Inborn genetic diseases
Other Variants in TWNK
rs2493633263 rs111033572 rs111033573 rs111033574 rs111033575 rs111033576 rs111033577 rs28937887 rs111033579 rs80356543
Ask Dr. Hemsworth about this variant