RS748513242 GCM2

Health Risk Chr 6:10881772
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Associated Conditions
Inborn genetic diseases
Hypoparathyroidism
familial isolated
2
Hyperparathyroidism 4
Familial hypoparathyroidism
Inborn genetic diseases
Hypoparathyroidism
familial isolated
2
Hyperparathyroidism 4
Familial hypoparathyroidism
Other Variants in GCM2
rs2113243235 rs2113242469 rs2113242520 rs2113257238 rs780323819 rs146395801 rs1779961435 rs532834782 rs2532749281 rs549670381
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