RS1060499695 THRB

Health Risk Chr 3:24127666
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What This Variant Does
"CLNSIG=4
Associated Conditions
Thyroid hormone resistance
generalized
autosomal dominant
Thyroid hormone resistance
generalized
autosomal dominant
Other Variants in THRB
rs121918686 rs121918688 rs121918687 rs387906515 rs121918700 rs121918690 rs28999969 rs28999970 rs28999971 rs121918691
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