RS201889708 TSHR

Health Risk Chr 14:81143400
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What This Variant Does
"CLNSIG=4
Associated Conditions
Inborn genetic diseases
Hypothyroidism due to TSH receptor mutations
Inborn genetic diseases
Hypothyroidism due to TSH receptor mutations
Other Variants in TSHR
rs121908859 rs121908860 rs121908861 rs121908862 rs121908863 rs121908864 rs28937584 rs121908865 rs121908866 rs121908867
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