RS148065361 SPTBN2

Health Risk Chr 11:66699059
Upload your DNA to see your genotype for this variant.
Associated Conditions
Autosomal recessive spinocerebellar ataxia 14
Spinocerebellar ataxia type 5
Inborn genetic diseases
Autosomal recessive spinocerebellar ataxia 14
Spinocerebellar ataxia type 5
Inborn genetic diseases
Other Variants in SPTBN2
rs1941485201 rs121918306 rs146859515 rs397514749 rs373728971 rs786205617 rs148207416 rs150159444 rs200956071 rs769987150
Ask Dr. Hemsworth about this variant