Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs76262710
rs76262710
RET
A 0.700 CausalMutation CLINVAR Revised American Thyroid Association guidelines for the management of medullary thyroid carcinoma. 25810047

2015
dbSNP: rs76262710
rs76262710
RET
A 0.700 CausalMutation CLINVAR Case report: a p.C618S RET proto-oncogene germline mutation in a large Chinese pedigree with familial medullary thyroid carcinoma. 22068382

2012
dbSNP: rs76262710
rs76262710
RET
A 0.700 CausalMutation CLINVAR Predominant RET Germline Mutations in Exons 10, 11, and 16 in Iranian Patients with Hereditary Medullary Thyroid Carcinoma. 21765987

2011
dbSNP: rs76262710
rs76262710
RET
A 0.700 CausalMutation CLINVAR A Korean family of familial medullary thyroid cancer with Cys618Ser RET germline mutation. 20119574

2010
dbSNP: rs76262710
rs76262710
RET
A 0.700 CausalMutation CLINVAR Medullary thyroid cancer: management guidelines of the American Thyroid Association. 19469690

2009
dbSNP: rs76262710
rs76262710
RET
A 0.700 CausalMutation CLINVAR Multiple endocrine neoplasia type 2 RET protooncogene database: repository of MEN2-associated RET sequence variation and reference for genotype/phenotype correlations. 19177457

2009
dbSNP: rs76262710
rs76262710
RET
A 0.700 CausalMutation CLINVAR RET proto-oncogene mutations in inherited and sporadic medullary thyroid cancer. 7849720

1994
dbSNP: rs76262710
rs76262710
RET
A 0.700 CausalMutation CLINVAR RET proto-oncogene mutations in French MEN 2A and FMTC families. 7874109

1994