RS1555198910 KMT2D

Health Risk Chr 12:49055006
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Associated Conditions
Inborn genetic diseases
Inborn genetic diseases
Other Variants in KMT2D
rs267607237 rs267607240 rs267607239 rs267607238 rs398123699 rs398123700 rs398123701 rs398123702 rs374418866 rs398123703
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