rs78378222, TP53

N. diseases: 37
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Glioma
CUI: C0017638
Disease: Glioma
0.720 GeneticVariation GWASCAT Sex-specific glioma genome-wide association study identifies new risk locus at 3p21.31 in females, and finds sex-differences in risk at 8q24.21. 29743610 2018
Glioma
CUI: C0017638
Disease: Glioma
0.720 GeneticVariation GWASCAT Genome-wide association study of glioma subtypes identifies specific differences in genetic susceptibility to glioblastoma and non-glioblastoma tumors. 28346443 2017
Glioma
CUI: C0017638
Disease: Glioma
0.720 GeneticVariation BEFREE As rs78378222 changes the polyadenylation signal of TP53 leading to impaired 3'-end processing of TP53 mRNA, the SNP has strong plausibility for being directly functional contributing to the aetiological basis of glioma. 23571737 2013
Glioma
CUI: C0017638
Disease: Glioma
0.720 GeneticVariation BEFREE The rs78378222 SNP is the first confirmed rare susceptibility variant in glioma. 22706378 2012