Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs77724903
rs77724903
RET
0.020 GeneticVariation BEFREE Primary hyperparathyroidism as the leading symptom in a patient with a Y791F RET mutation. 16356097

2005
dbSNP: rs77724903
rs77724903
RET
0.020 GeneticVariation BEFREE The key to diagnosis was recurrent HPT in a young male carrying RET mutation Y791F, a mutation not likely to give rise to recurrent HPT. 15870131

2005