RS1389916079 CWF19L1

Health Risk Chr 10:100235672
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Associated Conditions
Inborn genetic diseases
Inborn genetic diseases
Other Variants in CWF19L1
rs1330992740 rs201230582 rs1846978970 rs1846799593 rs2134307362 rs2134272638 rs1431707463 rs2493141408 rs1236392229 rs1424478086
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