Source: BEFREE

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs10069690
rs10069690
TERT
CUI: C0017636
Disease: Glioblastoma
Glioblastoma 		0.710 GeneticVariation BEFREE The minor alleles of rs2736100 and rs10069690 SNP's, located in intron 2 and the promotor regions, respectively, were associated with an increased risk of developing GBM (p = 0.004 and 0.001). 26143636

2015