RS1064796252 ITPR1

Health Risk Chr 3:4667476
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What This Variant Does
"CLNSIG=4
Associated Conditions
Inborn genetic diseases
ITPR1-related syndromic and non-syndromic hereditary ataxias
Spinocerebellar ataxia type 29
Inborn genetic diseases
ITPR1-related syndromic and non-syndromic hereditary ataxias
Spinocerebellar ataxia type 29
Other Variants in ITPR1
rs121912425 rs397514535 rs397514536 rs61757111 rs371988852 rs797044955 rs863224882 rs869312685 rs878853171 rs878853172
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