Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Myeloproliferative disease
CUI: C0027022
Disease: Myeloproliferative disease
0.040 GeneticVariation BEFREE TERT rs2736100 A>C SNP and JAK2 46/1 haplotype significantly contribute to the occurrence of JAK2 V617F and CALR mutated myeloproliferative neoplasms - a multicentric study on 529 patients. 27061303 2016
Myeloproliferative disease
CUI: C0027022
Disease: Myeloproliferative disease
0.040 GeneticVariation BEFREE Co-occurrence of Myeloproliferative Neoplasms and Solid Tumors Is Attributed to a Synergism Between Cytoreductive Therapy and the Common TERT Polymorphism rs2736100. 26487696 2016
Myeloproliferative disease
CUI: C0027022
Disease: Myeloproliferative disease
0.040 GeneticVariation BEFREE TERT rs2736100 genotypes are associated with differential risk of myeloproliferative neoplasms in Swedish and Chinese male patient populations. 27561898 2016
Myeloproliferative disease
CUI: C0027022
Disease: Myeloproliferative disease
0.040 GeneticVariation BEFREE The C allele of the rs2736100 single nucleotide polymorphism located in the second intron of the TERT gene has recently been identified as a susceptibility factor for myeloproliferative neoplasms (MPN) in the Icelandic population. 25196853 2014