RS748232676 SPTAN1

Health Risk Chr 9:128566795
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What This Variant Does
"CLNSIG=4
Associated Conditions
SPTAN1-related disorder
Spastic paraplegia 91
autosomal dominant
with or without cerebellar ataxia
Hereditary spastic paraplegia
Inborn genetic diseases
Early-infantile DEE
SPTAN1-related disorder
Spastic paraplegia 91
autosomal dominant
with or without cerebellar ataxia
Hereditary spastic paraplegia
Inborn genetic diseases
Early-infantile DEE
Other Variants in SPTAN1
rs398122865 rs377437879 rs138101005 rs41275900 rs147132904 rs72758823 rs187613754 rs202180736 rs587784431 rs370304886
Ask Dr. Hemsworth about this variant