Source: BEFREE

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs55705857
rs55705857
CCDC26
CUI: C0017638
Disease: Glioma
Glioma 		0.760 GeneticVariation BEFREE IDH1/2 mutated glioma has been associated with a germline risk variant, the rs55705857 G allele. 30823903

2019
dbSNP: rs55705857
rs55705857
CCDC26
CUI: C0017638
Disease: Glioma
Glioma 		0.760 GeneticVariation BEFREE Taken into consideration the limitations of this study, the present findings suggest a possible participation of rs891835, rs6470745, and rs55705857 as risk factors to develop glioma. 30778791

2019
dbSNP: rs55705857
rs55705857
CCDC26
CUI: C0017638
Disease: Glioma
Glioma 		0.760 GeneticVariation BEFREE Of the 6 variants located in 8q24, 2 have strong significant associations with the risk of glioma, including rs4295627 (P = .003, odds ratio [OR] = 1.21), rs55705857 (P = 2.31 × 10, OR = 3.54). 31277128

2019
dbSNP: rs55705857
rs55705857
CCDC26
CUI: C0017638
Disease: Glioma
Glioma 		0.760 GeneticVariation BEFREE IDH-mutant glioma specific association of rs55705857 located at 8q24.21 involves MYC deregulation. 27282637

2016
dbSNP: rs55705857
rs55705857
CCDC26
CUI: C0017638
Disease: Glioma
Glioma 		0.760 GeneticVariation BEFREE We also adjusted for the recently discovered 8q24 glioma risk locus rs55705857 G allele. 23361564

2013
dbSNP: rs55705857
rs55705857
CCDC26
CUI: C0017638
Disease: Glioma
Glioma 		0.760 GeneticVariation BEFREE Analysis by glioma subtype showed the association with rs55705857 confined to non-glioblastoma multiforme (non-GBM) tumours (P = 1.07 × 10(-67)). 23399484

2013