RS786205080 TSHR

Health Risk Chr 14:81092611
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What This Variant Does
"CLNSIG=5
Associated Conditions
Hypothyroidism due to TSH receptor mutations
Hypothyroidism due to TSH receptor mutations
Other Variants in TSHR
rs121908859 rs121908860 rs121908861 rs121908862 rs121908863 rs121908864 rs28937584 rs121908865 rs121908866 rs121908867
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