Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs79890926
rs79890926
RET
G 0.700 CausalMutation CLINVAR Revised American Thyroid Association guidelines for the management of medullary thyroid carcinoma. 25810047

2015
dbSNP: rs79890926
rs79890926
RET
G 0.700 CausalMutation CLINVAR Risk profiles and penetrance estimations in multiple endocrine neoplasia type 2A caused by germline RET mutations located in exon 10. 20979234

2011
dbSNP: rs79890926
rs79890926
RET
G 0.700 CausalMutation CLINVAR "Familial associations in medullary thyroid carcinoma with Hirschsprung disease: the role of the RET-C620 ""Janus"" genetic variation." 20152359

2010
dbSNP: rs79890926
rs79890926
RET
G 0.700 CausalMutation CLINVAR Medullary thyroid cancer: management guidelines of the American Thyroid Association. 19469690

2009
dbSNP: rs79890926
rs79890926
RET
G 0.700 CausalMutation CLINVAR Hirschsprung disease in MEN 2A: increased spectrum of RET exon 10 genotypes and strong genotype-phenotype correlation. 9384613

1998
dbSNP: rs79890926
rs79890926
RET
G 0.700 CausalMutation CLINVAR Rapid, nonradioactive screening for mutations in exons 10, 11, and 16 of the RET protooncogene associated with inherited medullary thyroid carcinoma. 9068588

1997
dbSNP: rs79890926
rs79890926
RET
G 0.700 CausalMutation CLINVAR Genetic testing in medullary thyroid carcinoma syndromes: mutation types and clinical significance. 9146685

1997