RS1085307573 TSHR

Health Risk Chr 14:81091091
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=4
Associated Conditions
Hypothyroidism due to TSH receptor mutations
Familial gestational hyperthyroidism
Familial hyperthyroidism due to mutations in TSH receptor
Hypothyroidism due to TSH receptor mutations
Familial gestational hyperthyroidism
Familial hyperthyroidism due to mutations in TSH receptor
Other Variants in TSHR
rs121908859 rs121908860 rs121908861 rs121908862 rs121908863 rs121908864 rs28937584 rs121908865 rs121908866 rs121908867
Ask Dr. Hemsworth about this variant