RS191759494 DUOX2
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What This Variant Does
"CLNSIG=4
Associated Conditions
Thyroid dyshormonogenesis 6
Familial thyroid dyshormonogenesis
Nongoitrous Euthyroid Hyperthyrotropinemia
Inborn genetic diseases
DUOX2-related disorder
Thyroid dyshormonogenesis 6
Familial thyroid dyshormonogenesis
Nongoitrous Euthyroid Hyperthyrotropinemia
Inborn genetic diseases
DUOX2-related disorder
Other Variants in DUOX2