Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs4646903
rs4646903
CYP1A1
0.050 GeneticVariation BEFREE Our study suggested that the presence of 'C' allele of rs4646903 (T>C) showed no risk and 'G' allele of rs1048943 (A>G) might be a leading allele to cause increased cervical cancer susceptibility due to significant association of CYP1A1m2 gene polymorphism. 28433806

2017
dbSNP: rs4646903
rs4646903
CYP1A1
0.050 GeneticVariation BEFREE We studied the association of CYP1A1 M1 (rs4646903) and COMT (rs4680) polymorphisms in 130 cervical cancer cases (c-cancer) and 179 controls. 26798414

2016
dbSNP: rs4646903
rs4646903
CYP1A1
0.050 GeneticVariation BEFREE rs4646903 minor alleles and interaction between rs4646903 and rs1048943 were associated with increased cervical cancer risk. 27265845

2016
dbSNP: rs4646903
rs4646903
CYP1A1
0.050 GeneticVariation BEFREE Association of CYP1A1 gene variants rs4646903 (T>C) and rs1048943 (A>G) with cervical cancer in a North Indian population. 24657182

2014
dbSNP: rs4646903
rs4646903
CYP1A1
0.050 GeneticVariation BEFREE An association with cervical cancer and high-grade dysplasia was found for the rare homozygous CC genotype (rs4646903) in CYP1A1 (odds ratio [OR], 8.862). 21897271

2011