RS387906515 THRB

Health Risk Chr 3:24127631
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What This Variant Does
"CLNSIG=5
Associated Conditions
Thyroid hormone resistance
generalized
autosomal dominant
autosomal recessive
Thyroid hormone resistance
generalized
autosomal dominant
autosomal recessive
Other Variants in THRB
rs121918686 rs121918688 rs121918687 rs121918700 rs121918690 rs28999969 rs28999970 rs28999971 rs121918691 rs121918701
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