RS1236392229 CWF19L1

Health Risk Chr 10:100256314
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Associated Conditions
Autosomal recessive spinocerebellar ataxia 17
Autosomal recessive spinocerebellar ataxia 17
Other Variants in CWF19L1
rs1431707463 rs772697259 rs201230582 rs1846978970 rs1846799593 rs2134307362 rs2134272638 rs2493141408 rs1424478086 rs772446354
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