RS530719719 DUOX2

Health Risk Chr 15:45101228
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What This Variant Does
"minor allele should be reclassified as benign according to
Associated Conditions
Familial thyroid dyshormonogenesis
Inborn genetic diseases
Nongoitrous Euthyroid Hyperthyrotropinemia
Congenital hypothyroidism
Thyroid dyshormonogenesis 6
DUOX2-related disorder
Familial thyroid dyshormonogenesis
Inborn genetic diseases
Nongoitrous Euthyroid Hyperthyrotropinemia
Congenital hypothyroidism
Thyroid dyshormonogenesis 6
DUOX2-related disorder
Other Variants in DUOX2
rs119472026 rs119472027 rs119472028 rs119472029 rs199752932 rs199589510 rs191759494 rs151261408 rs567500345 rs775863038
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