RS201196911 MCM3AP

Health Risk Chr 21:46236900
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Associated Conditions
Inborn genetic diseases
Inborn genetic diseases
Other Variants in MCM3AP
rs483352869 rs779248881 rs1569086477 rs1569073058 rs1569074992 rs373674344 rs1569072024 rs1569074977 rs763090302 rs1218260846
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