Gene: TERT ×
Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs797046041
rs797046041
TERT
C 0.700 GeneticVariation CLINVAR

dbSNP: rs35719940
rs35719940
TERT
0.020 GeneticVariation BEFREE In conclusion, the TERT A1062T variant is an independent negative prognostic factor in younger patients with acute myeloid leukemia and seems to predispose those patients to treatment-related toxicity. 28331964

2017
dbSNP: rs35719940
rs35719940
TERT
0.020 GeneticVariation BEFREE Therefore, molecular testing for TERT A1062T mutation in patients with AML is recommended in order to delineate their prognostic status. 25108601

2014
dbSNP: rs2736100
rs2736100
TERT
0.010 GeneticVariation BEFREE A significant association for increased risk of AML was found for TERT SNVs, rs2853669 (OR = 2.45, p = 0.00015) and rs2736100 (OR = 1.5, p = 0.03). 26298771

2015
dbSNP: rs2853669
rs2853669
TERT
0.010 GeneticVariation BEFREE We show that rs2853669 CC may be a risk factor for the development of AML that may also be used as a prognostic marker to identify high risk normal karyotype-AML (NK-AML) patients, for treatment guidance. 26298771

2015