rs78014899, RET

N. diseases: 12
Disease: Hyperparathyroidism ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Hyperparathyroidism
CUI: C0020502
Disease: Hyperparathyroidism
0.010 GeneticVariation BEFREE To date in this family the E768D mutation has not been associated with either phaeochromocytoma or hyperparathyroidism. 16736292 2006