RS104894699 KCNC3

Health Risk Chr 19:50323694
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What This Variant Does
"[OMIM:?]
Associated Conditions
Spinocerebellar ataxia type 13
Hereditary ataxia
Spinocerebellar ataxia type 13
Hereditary ataxia
Other Variants in KCNC3
rs927538730 rs764571894 rs1326942763 rs969993818 rs368232448 rs371116909 rs770686560 rs2513799489 rs568711737 rs558106649
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