RS142698837 TG
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What This Variant Does
"c.229G>
Associated Conditions
Iodotyrosyl coupling defect
Autoimmune thyroid disease
susceptibility to
3
TG-related disorder
Iodotyrosyl coupling defect
Autoimmune thyroid disease
susceptibility to
3
TG-related disorder
GWAS Studies (7)
| Trait | Risk Allele | OR / Beta | P-value | Study |
|---|---|---|---|---|
| Benign nodular goiter | A | OR: 1.06 | 9E-48 | PubMed |
| Benign nodular goiter | A | OR: 1.06 | 6E-46 | PubMed |
| Nontoxic nodular goiter (PheCode 241) | G | OR: 1.16 | 3E-31 | PubMed |
| Nontoxic uninodular goiter (PheCode 241.1) | G | OR: 1.17 | 5E-28 | PubMed |
| Nontoxic uninodular goiter (PheCode 241.1) | G | OR: 1.18 | 4E-22 | PubMed |
| Thyroid cancer | A | OR: 1.11 | 3E-20 | PubMed |
| Thyroid cancer | A | OR: 1.08 | 3E-18 | PubMed |
Other Variants in TG