Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs78014899
rs78014899
RET
0.010 GeneticVariation BEFREE To date in this family the E768D mutation has not been associated with either phaeochromocytoma or hyperparathyroidism. 16736292

2006