RS797044955 ITPR1

Health Risk Chr 3:4645673
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What This Variant Does
"CLNSIG=4
Associated Conditions
Inborn genetic diseases
Spinocerebellar ataxia type 29
Spinocerebellar ataxia type 15/16
Spinocerebellar ataxia type 29
Inborn genetic diseases
Spinocerebellar ataxia type 29
Spinocerebellar ataxia type 15/16
Spinocerebellar ataxia type 29
Other Variants in ITPR1
rs121912425 rs397514535 rs397514536 rs61757111 rs371988852 rs863224882 rs869312685 rs878853171 rs878853172 rs878853173
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