Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1047972
rs1047972
AURKA
0.010 GeneticVariation BEFREE For the V57I SNP, neither the homozygous (AA) nor the heterozygous (GA) variant genotypes were associated with significantly altered risk for uterine cancer (OR 0.76; 95% CI 0.18-3.25 and OR 0.88; 95% CI 0.52-1.49). 17599395

2007
dbSNP: rs142155101
rs142155101
BARD1
0.710 GeneticVariation BEFREE Along with the G2355C (S761N) missense mutation previously identified in a uterine cancer, we found two other variants in breast cancers, T2006C (C645R) and A2286G (I738V). 16061562

2005
dbSNP: rs142155101
rs142155101
BARD1
0.710 GeneticVariation UNIPROT

dbSNP: rs2273535
rs2273535
AURKA
0.010 GeneticVariation BEFREE Our study demonstrates that STK15 F31I SNP is associated with an increased risk for uterine cancer. 17599395

2007
dbSNP: rs587779157
rs587779157
MSH2
G 0.700 CausalMutation CLINVAR