rs1799939, RET

N. diseases: 27
Disease: Pheochromocytoma ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Pheochromocytoma
CUI: C0031511
Disease: Pheochromocytoma
0.020 GeneticVariation BEFREE The findings propose a classification of 15 of the 26 VUS in RET without any well-defined risk profiles and suggest that the G691S SNP, or a combination of SNPs, may be associated with the development of PHEO. 28946813 2017
Pheochromocytoma
CUI: C0031511
Disease: Pheochromocytoma
0.020 GeneticVariation BEFREE We did not observe any association between the frequencies of L769L, S836S, or S904S/G691S variants and PHEO development (all P>0.05). 24616415 2014