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 None of the K666N DNA variant carriers had evidence of primary hyperparathyroidism or pheochromocytoma. 27673361

2016