RS566911022 MNX1

Health Risk Chr 7:157005831
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Associated Conditions
Inborn genetic diseases
Inborn genetic diseases
Other Variants in MNX1
rs2537780168 rs121912546 rs2537781329 rs121912547 rs1563700090 rs1563700419 rs121912548 rs121912549 rs1064794653 rs1064796665
Ask Dr. Hemsworth about this variant