Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1056836
rs1056836
0.050 GeneticVariation BEFREE The GSTA1 rs3957356 TT (HR = 5.36, 95% CI = 2.39-12.0) and CYP1B1 rs1056836 CC (HR = 7.24, 95% CI = 3.51-14.9) were significantly associated with CRC risk when compared to wild-type CC and GG genotypes, respectively. 28714190

2018

dbSNP: rs1056836
rs1056836
0.050 GeneticVariation BEFREE The previous published data on the association between CYP1A2*F (rs762551), CYP1B1 Leu432Val (rs1056836), Asn453Ser (rs180040), and Arg48Gly (rs10012) polymorphisms and colorectal cancer risk remained controversial. 25115775

2014

dbSNP: rs1056836
rs1056836
0.050 GeneticVariation BEFREE No association is found between the CYP1B1 Leu432Val polymorphism and risk of CRC among Caucasians. 22190224

2012

dbSNP: rs1056836
rs1056836
0.050 GeneticVariation BEFREE Haplotypes of rs1056827 and rs10012 or rs1056827 and rs1056836 revealed an association with colorectal cancer which was significantly stronger in the homozygous carriers. 20701755

2010

dbSNP: rs1056836
rs1056836
0.050 GeneticVariation BEFREE Through an association study based on 1,023 cases and 1,121 controls, we examined the influence on CRC risk of environmental factors coanalyzed with combinations of six single nucleotide polymorphisms located in cytochrome P450 genes (c.-163A>C and c.1548T>C in CYP1A2, g.-1293G>C and g.-1053C>T in CYP2E1, c.1294C>G in CYP1B1, and c.430C>T in CYP2C9). 17627011

2007

dbSNP: rs1056827
rs1056827
0.020 GeneticVariation BEFREE Moreover, significant interactions were observed between NAT1 acetylation and CYP1B1 rs1056827 and meat consumption.Our results suggest that xenobiotic-metabolizing SNPs are not only associated with CRC risk in patients with Lynch syndrome in Taiwan but also interact with meat consumption to modify the disease risk.Environ.Mol.Mutagen.59:69-78, 2018.© 2017 Wiley Periodicals, Inc. 28714190

2018

dbSNP: rs10012
rs10012
0.020 GeneticVariation BEFREE In summary, this meta-analysis indicates that CYP1A2*F, CYP1B1 Leu432Val, Asn453Ser, and Arg48Gly polymorphisms do not support an association with colorectal cancer, and further studies are needed to investigate the association. 25115775

2014

dbSNP: rs1800440
rs1800440
0.020 GeneticVariation BEFREE The previous published data on the association between CYP1A2*F (rs762551), CYP1B1 Leu432Val (rs1056836), Asn453Ser (rs180040), and Arg48Gly (rs10012) polymorphisms and colorectal cancer risk remained controversial. 25115775

2014

dbSNP: rs1800440
rs1800440
0.020 GeneticVariation BEFREE No association was found between the CYP1B1 Asn453Ser polymorphism and risk of CRC among Caucasians. 22459615

2012

dbSNP: rs10012
rs10012
0.020 GeneticVariation BEFREE Haplotypes of rs1056827 and rs10012 or rs1056827 and rs1056836 revealed an association with colorectal cancer which was significantly stronger in the homozygous carriers. 20701755

2010

dbSNP: rs1056827
rs1056827
0.020 GeneticVariation BEFREE Haplotypes of rs1056827 and rs10012 or rs1056827 and rs1056836 revealed an association with colorectal cancer which was significantly stronger in the homozygous carriers. 20701755

2010

dbSNP: rs760025060
rs760025060
0.010 GeneticVariation BEFREE Overall, the variant genotypes (GG and GA) of the 453 A/G were not associated with CRC risk when compared with the wild-type AA homozygote (GG vs AA, OR=0.94, 95% CI=0.77-1.14; GA vs AA, OR=0.99, 95% CI=0.87-1.12). 22459615

2012

dbSNP: rs162558
rs162558
0.010 GeneticVariation BEFREE There was a suggestion of increased risk, albeit insignificant after correction for multiple testing, of CRC for individuals homozygous for CYP1B1 rs162558 and heterozygous for CYP1A2 rs2069522 (odds ratio [OR] = 1.36, 95% confidence interval [CI]: 1.03-1.80 and OR = 1.34, 95% CI: 1.00-1.79 respectively). 17615053

2007