rs121908866(G;G)
From SNPedia
common in clinvar |
Is a | genotype |
of | rs121908866 |
Gene | TSHR, LOC101928431, LOC101928462 |
Chromosome | 14 |
Position | 81,143,695 |
mentioned | by |
Magnitude | 0 |
Repute | Good |
Geno | Mag | Summary |
---|---|---|
(A;G) | 3 | Carrier of a congenital hypothyroidism mutation; 3.3x higher risk for hypothyroidism |
(G;G) | 0 | common in clinvar |