RS1557194018 CLCN5

Health Risk Chr X:50086687
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Associated Conditions
Inborn genetic diseases
Inborn genetic diseases
Other Variants in CLCN5
rs151340620 rs151340621 rs151340622 rs151340623 rs151340624 rs151340625 rs151340626 rs151340627 rs1569540520 rs151340628
Ask Dr. Hemsworth about this variant