rs146646971, RET

N. diseases: 7
Disease: Hyperparathyroidism, Primary ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Hyperparathyroidism, Primary
CUI: C0221002
Disease: Hyperparathyroidism, Primary
0.010 GeneticVariation BEFREE None of the K666N DNA variant carriers had evidence of primary hyperparathyroidism or pheochromocytoma. 27673361 2016