RS1969141028 KMT2B

Health Risk Chr 19:35720473
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Associated Conditions
Inborn genetic diseases
Inborn genetic diseases
Other Variants in KMT2B
rs1057519278 rs1057519279 rs1057519280 rs1057519281 rs1057519282 rs1057519283 rs1057519284 rs1057519285 rs1085307751 rs190929421
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