rs121908866(A;G)
From SNPedia
| Carrier of a congenital hypothyroidism mutation; 3.3x higher risk for hypothyroidism |
| Is a | genotype |
| of | rs121908866 |
| Gene | TSHR, LOC101928431, LOC101928462 |
| Chromosome | 14 |
| Position | 81,143,695 |
| mentioned | by |
| Magnitude | 3 |
| Repute | Bad |
| Geno | Mag | Summary |
|---|---|---|
| (A;G) | 3 | Carrier of a congenital hypothyroidism mutation; 3.3x higher risk for hypothyroidism |
| (G;G) | 0 | common in clinvar |
Unaffected in absence of a second TSHR gene mutation; see links and text via main rs-page
