RS121912648 TG
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What This Variant Does
"[OMIM:?]
Associated Conditions
Iodotyrosyl coupling defect
Congenital hypothyroidism
Autoimmune thyroid disease
susceptibility to
3
TG-related disorder
Iodotyrosyl coupling defect
Congenital hypothyroidism
Autoimmune thyroid disease
susceptibility to
3
TG-related disorder
GWAS Studies (10)
| Trait | Risk Allele | OR / Beta | P-value | Study |
|---|---|---|---|---|
| Hypothyroidism (PheCode 244) | C | OR: 1.3 | 9E-39 | PubMed |
| Hypothyroidism NOS (PheCode 244.4) | C | OR: 1.3 | 5E-38 | PubMed |
| Hypothyroidism (PheCode 244) | C | OR: 1.31 | 2E-33 | PubMed |
| Hypothyroidism NOS (PheCode 244.4) | C | OR: 1.31 | 4E-33 | PubMed |
| Hypothyroidism | T | OR: 0.88 | 2E-19 | PubMed |
| Thyroid problems | C | OR: 1.09 | 9E-16 | PubMed |
| Hypothyroidism | T | OR: 0.86 | 3E-14 | PubMed |
| Takes medication for Thyroid problems? | C | OR: 1.09 | 7E-14 | PubMed |
| Takes medication for Thyroid problems? | C | OR: 1.1 | 3E-13 | PubMed |
| Hypothyroidism | — | OR: 3.66 | 7E-9 | PubMed |
Other Variants in TG