RS866945292 SPTBN2

Health Risk Chr 11:66685924
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Associated Conditions
Inborn genetic diseases
Autosomal recessive spinocerebellar ataxia 14
Inborn genetic diseases
Autosomal recessive spinocerebellar ataxia 14
Other Variants in SPTBN2
rs1941485201 rs121918306 rs146859515 rs397514749 rs373728971 rs786205617 rs148207416 rs150159444 rs200956071 rs769987150
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