Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs146646971
rs146646971
RET
0.020 GeneticVariation BEFREE Here we report a case of a homozygous RET K666N mutation leading to coincident MTC and PHEO. 29408964

2018
dbSNP: rs146646971
rs146646971
RET
0.020 GeneticVariation BEFREE Given the potential benefit associated with early detection of aberrant C-cell growth, and the noninvasive nature of genetic testing, "at risk" individuals should be screened, and if the K666N variant is identified, they should be managed using a personalized screening approach for detection of MTC. 27673361

2016