RS137852693 NKX2-1

Health Risk Chr 14:36517871
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What This Variant Does
"[OMIM:?]
Associated Conditions
Brain-lung-thyroid syndrome
Inborn genetic diseases
Benign hereditary chorea
Brain-lung-thyroid syndrome
Inborn genetic diseases
Benign hereditary chorea
Other Variants in NKX2-1
rs28936671 rs28936672 rs387906404 rs137852692 rs587776707 rs587776708 rs137852694 rs587776709 rs537209983 rs863225300
Ask Dr. Hemsworth about this variant