RS121908863 TSHR

Health Risk Chr 14:81092547
Upload your DNA to see your genotype for this variant.
What This Variant Does
"[OMIM:?]
Associated Conditions
Hypothyroidism due to TSH receptor mutations
Familial hyperthyroidism due to mutations in TSH receptor
Familial gestational hyperthyroidism
Hypothyroidism due to TSH receptor mutations
Hypothyroidism due to TSH receptor mutations
Familial hyperthyroidism due to mutations in TSH receptor
Familial gestational hyperthyroidism
Hypothyroidism due to TSH receptor mutations
Other Variants in TSHR
rs121908859 rs121908860 rs121908861 rs121908862 rs121908864 rs28937584 rs121908865 rs121908866 rs121908867 rs121908869
Ask Dr. Hemsworth about this variant