RS150159444 SPTBN2

Health Risk Chr 11:66721079
Upload your DNA to see your genotype for this variant.
Associated Conditions
Spinocerebellar ataxia type 5
Autosomal recessive spinocerebellar ataxia 14
SPTBN2-related disorder
Uterine carcinosarcoma
Spinocerebellar ataxia type 5
Autosomal recessive spinocerebellar ataxia 14
SPTBN2-related disorder
Uterine carcinosarcoma
Other Variants in SPTBN2
rs1941485201 rs121918306 rs146859515 rs397514749 rs373728971 rs786205617 rs148207416 rs200956071 rs769987150 rs797046005
Ask Dr. Hemsworth about this variant