RS121908869 TSHR
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What This Variant Does
"[OMIM:?]
Associated Conditions
Hypothyroidism due to TSH receptor mutations
Epilepsy
Developmental delay
autistic features
Familial hyperthyroidism due to mutations in TSH receptor
Hypothyroidism due to TSH receptor mutations
Epilepsy
Developmental delay
autistic features
Familial hyperthyroidism due to mutations in TSH receptor
Other Variants in TSHR