RS28936672 NKX2-1
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What This Variant Does
"[OMIM:CHOREA, BENIGN HEREDITARY]
Associated Conditions
Benign hereditary chorea
Brain-lung-thyroid syndrome
NKX2-1-related disorder
Benign hereditary chorea
Benign hereditary chorea
Brain-lung-thyroid syndrome
NKX2-1-related disorder
Benign hereditary chorea
Other Variants in NKX2-1