Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs377767434
rs377767434
Entrez Id: 5979
Gene Symbol: RET
RET
CUI: C1833921
Disease:
Familial medullary thyroid carcinoma
TGGAGTGTGA 0.700 CausalMutation CLINVAR A novel 9-base pair duplication in RET exon 8 in familial medullary thyroid carcinoma. 10323403 1999