Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs376066276
rs376066276
0.010 GeneticVariation BEFREE Collectively, our study demonstrates that the R64Q mutation abolishes the suppressive effects of TRIM21 on the invasion of breast cancer cells. 31622717

2020

dbSNP: rs772893086
rs772893086
0.010 GeneticVariation BEFREE This study demonstrates that IDH1 R132H mutation with increased oncometabolite R-2HG in PCa cells may play important roles to increase PCa cell invasion. 31846689

2020

dbSNP: rs1046282
rs1046282
0.010 GeneticVariation BEFREE The results of clinicopathologic analysis showed that A allele at the rs737241 locus could increase the expression level of AFP (P = .007), the rs1046282 mutation C allele could increase the AFP expression level (P = .011), rs4024 locus mutation A allele could reduce the risk of vascular invasion (P = .013), rs3212948 locus mutation T allele could reduce the differentiation of liver cancer (P = .022), rs1046282 locus C allele could reduce the DNA load of hepatitis B virus (P = .035), and rs735482 A allele could increase the tumor size in HCC (P = .037).The SNPs in rs737241 for AFP gene may correlate with the occurrence of HCC. 30946366

2019

dbSNP: rs11064
rs11064
0.010 GeneticVariation BEFREE It also showed that SNP rs11064 was associated with advanced FIGO stage (P = 0.001), deep myometrial invasion (P = 0.047), and lymph node metastasis (P = 0.048) under the codominant model in ECs. 31043860

2019

dbSNP: rs11801299
rs11801299
0.010 GeneticVariation BEFREE RB patients carrying AA genotype and A allele at rs11801299 were more likely to have tumor invasion and poor differentiation. 30597480

2019

dbSNP: rs1194338
rs1194338
0.010 GeneticVariation BEFREE Female patients and patients with a smoking habit who carried the CA + AA genotype of rs1194338 had a lower risk of developing vascular invasion (p = 0.049) and a high Child-Pugh grade (B or C) (p = 0.036), respectively. 31500187

2019

dbSNP: rs121913412
rs121913412
0.010 GeneticVariation BEFREE Our results revealed that a lower dose of sorafenib was able to inhibit cell viability, migration, and invasion of wild-type and T41A-mutated DTs. 30980399

2019

dbSNP: rs145204276
rs145204276
0.010 GeneticVariation BEFREE The results shown that patients who carries genotype ins/del or del/del at SNP rs145204276 showed decreased risk of pathological lymph node metastasis disease (OR=0.545, p=0.043) and risk of seminal vesicle invasion (OR=0.632, p=0.022) comparing to with genotype ins/ins. 31673232

2019

dbSNP: rs1800625
rs1800625
0.010 GeneticVariation BEFREE Subgroup analysis revealed that among UCC patients aged younger than 65 years, those with a C allele at rs1800625 had a higher incidence of muscle invasive tumor and lymph node invasion. 30824390

2019

dbSNP: rs2070744
rs2070744
0.010 GeneticVariation BEFREE However, cervical cancer patients with genotypes TC/CC in eNOS SNP rs2070744 carried less risk of advanced stage [odds ratios (OR) = 0.30, 95% confidence interval (CI)=0.09-0.97, <i>p</i>=0.036], parametrium invasion (OR=0.16, 95% CI=0.02-0.75, <i>p</i>=0.009) and pelvic lymph node metastasis (OR=0.12, 95% CI=0.01-0.89, <i>p</i>=0.016). 31258766

2019

dbSNP: rs3212948
rs3212948
0.010 GeneticVariation BEFREE The results of clinicopathologic analysis showed that A allele at the rs737241 locus could increase the expression level of AFP (P = .007), the rs1046282 mutation C allele could increase the AFP expression level (P = .011), rs4024 locus mutation A allele could reduce the risk of vascular invasion (P = .013), rs3212948 locus mutation T allele could reduce the differentiation of liver cancer (P = .022), rs1046282 locus C allele could reduce the DNA load of hepatitis B virus (P = .035), and rs735482 A allele could increase the tumor size in HCC (P = .037).The SNPs in rs737241 for AFP gene may correlate with the occurrence of HCC. 30946366

2019

dbSNP: rs371769427
rs371769427
0.010 GeneticVariation BEFREE U2AF1 S34F induced expression of genes involved in the epithelial-mesenchymal transition (EMT) and increased tumor cell invasion. 31836708

2019

dbSNP: rs3741219
rs3741219
0.010 GeneticVariation BEFREE Meanwhile, cervical cancer patients with AA/AG in rs3741219 also had less risk to develop pelvic lymph node metastasis (OR: 0.17, 95% CI: 0.05-0.63, <i>p</i>=0.008), large tumor (OR: 0.17, 95% CI: 0.04-0.82, <i>p</i>=0.014) as well as parametrium (OR: 0.26, 95% CI: 0.07-0.95, <i>p</i>=0.045) and vagina invasion (OR: 0.25, 95% CI: 0.07-0.91, <i>p</i>=0.041, as compared to those with GG. 31772651

2019

dbSNP: rs3829078
rs3829078
CA9
0.010 GeneticVariation BEFREE Furthermore, patients with CaP with an initial PSA level ≤10 ng/ml who carried at least one G allele at CA9 rs3829078 had a 4.532-fold and 3.484-fold risk of lymph node metastasis and lymphovascular invasion, respectively. 31155437

2019

dbSNP: rs387906698
rs387906698
0.010 GeneticVariation BEFREE It showed that migration and invasion were significantly increased in R116C-bearing PANC-1 cells compared with wild type counterparts. 31521106

2019

dbSNP: rs4024
rs4024
AFP
0.010 GeneticVariation BEFREE The results of clinicopathologic analysis showed that A allele at the rs737241 locus could increase the expression level of AFP (P = .007), the rs1046282 mutation C allele could increase the AFP expression level (P = .011), rs4024 locus mutation A allele could reduce the risk of vascular invasion (P = .013), rs3212948 locus mutation T allele could reduce the differentiation of liver cancer (P = .022), rs1046282 locus C allele could reduce the DNA load of hepatitis B virus (P = .035), and rs735482 A allele could increase the tumor size in HCC (P = .037).The SNPs in rs737241 for AFP gene may correlate with the occurrence of HCC. 30946366

2019

dbSNP: rs735482
rs735482
0.010 GeneticVariation BEFREE The results of clinicopathologic analysis showed that A allele at the rs737241 locus could increase the expression level of AFP (P = .007), the rs1046282 mutation C allele could increase the AFP expression level (P = .011), rs4024 locus mutation A allele could reduce the risk of vascular invasion (P = .013), rs3212948 locus mutation T allele could reduce the differentiation of liver cancer (P = .022), rs1046282 locus C allele could reduce the DNA load of hepatitis B virus (P = .035), and rs735482 A allele could increase the tumor size in HCC (P = .037).The SNPs in rs737241 for AFP gene may correlate with the occurrence of HCC. 30946366

2019

dbSNP: rs737241
rs737241
AFP
0.010 GeneticVariation BEFREE The results of clinicopathologic analysis showed that A allele at the rs737241 locus could increase the expression level of AFP (P = .007), the rs1046282 mutation C allele could increase the AFP expression level (P = .011), rs4024 locus mutation A allele could reduce the risk of vascular invasion (P = .013), rs3212948 locus mutation T allele could reduce the differentiation of liver cancer (P = .022), rs1046282 locus C allele could reduce the DNA load of hepatitis B virus (P = .035), and rs735482 A allele could increase the tumor size in HCC (P = .037).The SNPs in rs737241 for AFP gene may correlate with the occurrence of HCC. 30946366

2019

dbSNP: rs738791
rs738791
0.010 GeneticVariation BEFREE Although CT/TT genotype of MMP-11 gene rs738791 tended to increase the risk of developing stage II disease at least (p=0.035; OR: 2.16, 95% CI: 1.05-4.44) and deep stromal invasion more than 10 mm (p=0.043; OR: 2.08, 95% CI: 1.02-4.26) with CC as a reference in patients with uterine cervical cancer. 31337950

2019

dbSNP: rs1057519788
rs1057519788
0.010 GeneticVariation BEFREE Combination of Twist1 siRNA and crizotinib significantly reduced cell vitality, inhibited cell invasion and migration, and promoted apoptosis in A549-CD74-ROS1 G2032R mutation cells. 29477381

2018

dbSNP: rs12918952
rs12918952
0.010 GeneticVariation BEFREE Cervical cancer patients with GA/AA in rs12918952 tend to have more risk to develop parametrium invasion and pelvic lymph node metastasis. 30013442

2018

dbSNP: rs1431090090
rs1431090090
0.010 GeneticVariation BEFREE Functionally, GATA3-acetylation mimics K119Q mutant was found to inhibit lung adenocarcinoma cell migration and invasion with concomitant downregulation of EMT-controlling transcriptional factors Slug, Zeb1 and Zeb2. 29453984

2018

dbSNP: rs1646724
rs1646724
0.010 GeneticVariation BEFREE Further investigation revealed that rs1646724 may affect expression of SLC35B4, which encodes a glycosyltransferase, and that down-regulation of SLC35B4 by transfecting short hairpin RNA in DU145 human prostate cancer cell suppressed proliferation, migration and invasion. 29682886

2018

dbSNP: rs1799983
rs1799983
0.010 GeneticVariation BEFREE With the subgroup of EGFR L858R mutation, variant genotypes (GT + TT) of <i>eNOS</i> 894 G/T were significantly associated with lymph node invasion. 30026850

2018

dbSNP: rs1800624
rs1800624
0.010 GeneticVariation BEFREE Moreover, cervical cancer patients with genotypes TA/AA in rs1800624 exhibited a lower risk of parametrium invasion, moderate-to-poor cell differentiation, and pelvic lymph node metastasis. 30410591

2018