RS146859515 SPTBN2

Health Risk Chr 11:66705395
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=5
Associated Conditions
Autosomal recessive spinocerebellar ataxia 14
Autosomal recessive spinocerebellar ataxia 14
Other Variants in SPTBN2
rs1941485201 rs121918306 rs397514749 rs373728971 rs786205617 rs148207416 rs150159444 rs200956071 rs769987150 rs797046005
Ask Dr. Hemsworth about this variant