RS121908871 TSHR
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What This Variant Does
"[OMIM:?]
Associated Conditions
Hypothyroidism due to TSH receptor mutations
Familial hyperthyroidism due to mutations in TSH receptor
Familial gestational hyperthyroidism
Congenital hypothyroidism
Hypothyroidism due to TSH receptor mutations
Familial hyperthyroidism due to mutations in TSH receptor
Familial gestational hyperthyroidism
Congenital hypothyroidism
Other Variants in TSHR