RS4774518 DUOXA2

Health Risk Chr 15:45117274
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What This Variant Does
"[OMIM:?]
Associated Conditions
Thyroglobulin synthesis defect
Inborn genetic diseases
Familial thyroid dyshormonogenesis
Thyroglobulin synthesis defect
Inborn genetic diseases
Familial thyroid dyshormonogenesis
Other Variants in DUOXA2
rs778410503 rs201506037 rs201808443 rs1555414714 rs1555415049 rs767104514 rs769776095 rs781126484 rs770148072 rs974496530
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