RS1048886135 KMT2C

Health Risk Chr 7:152156249
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Associated Conditions
Inborn genetic diseases
Inborn genetic diseases
Other Variants in KMT2C
rs587777073 rs12674022 rs587778491 rs587778494 rs200297010 rs587778495 rs138845109 rs140626076 rs143269206 rs545625106
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