RS397516793 MAP2K1

Health Risk Chr 15:66436842
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What This Variant Does
"aka c.388T&gt
Associated Conditions
Cardio-facio-cutaneous syndrome
Inborn genetic diseases
Cardiofaciocutaneous syndrome 3
Cardio-facio-cutaneous syndrome
Inborn genetic diseases
Cardiofaciocutaneous syndrome 3
Other Variants in MAP2K1
rs121908594 rs121908595 rs121908596 rs1428775799 rs730880503 rs397516792 rs730880508 rs730880507 rs397516790 rs727504317
Ask Dr. Hemsworth about this variant