RS1064794653 MNX1

Health Risk Chr 7:157005841
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What This Variant Does
"CLNSIG=4
Associated Conditions
Inborn genetic diseases
MNX1-related disorder
Inborn genetic diseases
MNX1-related disorder
Other Variants in MNX1
rs2537780168 rs121912546 rs2537781329 rs121912547 rs1563700090 rs1563700419 rs121912548 rs121912549 rs1064796665 rs1554594329
Ask Dr. Hemsworth about this variant