RS201506037 DUOXA2

Health Risk Chr 15:45115858
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What This Variant Does
"CLNSIG=4
Associated Conditions
Thyroglobulin synthesis defect
Congenital hypothyroidism
Inborn genetic diseases
DUOXA2-related disorder
Thyroglobulin synthesis defect
Congenital hypothyroidism
Inborn genetic diseases
DUOXA2-related disorder
Other Variants in DUOXA2
rs4774518 rs778410503 rs201808443 rs1555414714 rs1555415049 rs767104514 rs769776095 rs781126484 rs770148072 rs974496530
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