Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1553278844
rs1553278844
Entrez Id: 79577;100302163
Gene Symbol: CDC73;MIR1278
CDC73;MIR1278
CUI: C0687150
Disease:
Parathyroid Gland Adenocarcinoma
T 0.700 CausalMutation CLINVAR Frequent large germline HRPT2 deletions in a French National cohort of patients with primary hyperparathyroidism. 23293331 2013