Variant Gene Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs142155101
rs142155101
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

2006

dbSNP: rs142155101
rs142155101
0.710 GeneticVariation UNIPROT Mutations in the BRCA1-associated RING domain (BARD1) gene in primary breast, ovarian and uterine cancers. 9425226

1998

dbSNP: rs1047972
rs1047972
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: rs2273535
rs2273535
0.010 GeneticVariation BEFREE STK15 F31I polymorphism is associated with increased uterine cancer risk: a pilot study. 17599395

2007

dbSNP: rs28930073
rs28930073
0.010 GeneticVariation BEFREE The MLH1 D132H risk variant has significantly lower allele frequency in American compared with Israeli cancer patients and, alone, is unlikely to explain significant amounts of American sporadic colorectal cancer or uterine cancer susceptibility. 15991064

2005