RS797044872 KCNC3

Health Risk Chr 19:50323685
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What This Variant Does
"CLNSIG=5
Associated Conditions
Inborn genetic diseases
Spinocerebellar ataxia type 13
Inborn genetic diseases
Spinocerebellar ataxia type 13
Other Variants in KCNC3
rs927538730 rs764571894 rs1326942763 rs969993818 rs368232448 rs371116909 rs770686560 rs2513799489 rs568711737 rs558106649
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