RS121908872 TSHR
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What This Variant Does
"[OMIM:?]
Associated Conditions
Hypothyroidism due to TSH receptor mutations
Inborn genetic diseases
Familial gestational hyperthyroidism
Familial hyperthyroidism due to mutations in TSH receptor
TSHR-related disorder
Hypothyroidism due to TSH receptor mutations
Inborn genetic diseases
Familial gestational hyperthyroidism
Familial hyperthyroidism due to mutations in TSH receptor
TSHR-related disorder
GWAS Studies (1)
| Trait | Risk Allele | OR / Beta | P-value | Study |
|---|---|---|---|---|
| Thyroid stimulating hormone levels | A | OR: 1.63 | 2E-31 | PubMed |
Other Variants in TSHR