RS121908866 TSHR
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What This Variant Does
"[OMIM:?]
Associated Conditions
Hypothyroidism due to TSH receptor mutations
Inborn genetic diseases
TSHR-related disorder
Familial hyperthyroidism due to mutations in TSH receptor
Familial gestational hyperthyroidism
Congenital hypothyroidism
Hypothyroidism due to TSH receptor mutations
Inborn genetic diseases
TSHR-related disorder
Familial hyperthyroidism due to mutations in TSH receptor
Familial gestational hyperthyroidism
Congenital hypothyroidism
GWAS Studies (1)
| Trait | Risk Allele | OR / Beta | P-value | Study |
|---|---|---|---|---|
| Hypothyroidism | A | OR: 2.04 | 2E-28 | PubMed |
Population Frequencies
gnomAD ALL
0%
Other Variants in TSHR