RS1057519733 MAP2K1

Health Risk Chr 15:66481793
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What This Variant Does
"CLNSIG=5
Associated Conditions
Inborn genetic diseases
Cardiofaciocutaneous syndrome 3
Cardiofaciocutaneous syndrome 3
Inborn genetic diseases
Cardiofaciocutaneous syndrome 3
Cardiofaciocutaneous syndrome 3
Other Variants in MAP2K1
rs121908594 rs121908595 rs121908596 rs1428775799 rs730880503 rs397516792 rs730880508 rs397516793 rs730880507 rs397516790
Ask Dr. Hemsworth about this variant