RS879255653 CWF19L1

Health Risk Chr 10:100245817
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What This Variant Does
"CLNSIG=5
Associated Conditions
Autosomal recessive spinocerebellar ataxia 17
Autosomal recessive spinocerebellar ataxia 17
Other Variants in CWF19L1
rs1330992740 rs201230582 rs1846978970 rs1846799593 rs2134307362 rs2134272638 rs1431707463 rs2493141408 rs1236392229 rs1424478086
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