Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs75234356
rs75234356
RET
0.020 GeneticVariation BEFREE Our report suggests that cases with S891A mutation, akin to those with other RET mutations, require screening for pheochromocytoma. 24449023

2014

dbSNP: rs75234356
rs75234356
RET
0.020 GeneticVariation BEFREE S891A mutation caused medullary thyroid cancer (MTC) in 69.4%, pheochromocytoma in 2.8%, and parathyroid hyperplasia in 8.3% of the 36 patients of this case series and in 63.5, 4.1, and 4.1%, respectively, for the entire groups of 74 patients. 20554711

2010