rs1799939, RET

N. diseases: 27
Disease: THYROID CARCINOMA, SPORADIC MEDULLARY ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
THYROID CARCINOMA, SPORADIC MEDULLARY
CUI: C1833929
Disease: THYROID CARCINOMA, SPORADIC MEDULLARY
0.030 GeneticVariation BEFREE Our data demonstrate that the RET G691S variant could modulate the age of onset of sMTC as demonstrated previously for familial tumours. 18331611 2008
THYROID CARCINOMA, SPORADIC MEDULLARY
CUI: C1833929
Disease: THYROID CARCINOMA, SPORADIC MEDULLARY
0.030 GeneticVariation BEFREE On the other hand, the frequency and distribution of G691S/S904S variants were similar in both groups of study, leading to exclude their role in sMTC in our series. 16646689 2006
THYROID CARCINOMA, SPORADIC MEDULLARY
CUI: C1833929
Disease: THYROID CARCINOMA, SPORADIC MEDULLARY
0.030 GeneticVariation BEFREE RET exon 11 (G691S) polymorphism is significantly more frequent in sporadic medullary thyroid carcinoma than in the general population. 15240649 2004