Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs10009228
rs10009228
CUI: C0178874
Disease: Tumor Progression
Tumor Progression
0.010 GeneticVariation BEFREE A SNP in the alpha9 subunit, the G allele of rs10009228 (alpha9, A>G) shows a significant trend in the combined cohort, indicating that this allele constitutes a risk factor for neoplastic progression. 22406075

2012

dbSNP: rs1042028
rs1042028
CUI: C0178874
Disease: Tumor Progression
Tumor Progression
0.010 GeneticVariation BEFREE Accumulating data indicates that the polymorphism rs9282861 (R213H) is responsible for inefficient enzymatic activity and associated with cancer progression. 31835852

2019

dbSNP: rs104893626
rs104893626
CUI: C0178874
Disease: Tumor Progression
Tumor Progression
0.010 GeneticVariation BEFREE C1013G/CXCR4 acts as a driver mutation of tumor progression and modulator of drug resistance in lymphoplasmacytic lymphoma. 24711662

2014

dbSNP: rs104894230
rs104894230
CUI: C0178874
Disease: Tumor Progression
Tumor Progression
0.010 GeneticVariation BEFREE The transformed phenotype of IOE(CMYC) cells was further enhanced in concert with KRAS(G12V)/BRAF(V600E) expression, as in vitro analyses indicated that IOE(CMYC) cells had undergone morphological and phenotypic changes characteristic of neoplastic progression. 21859834

2011

dbSNP: rs1057519710
rs1057519710
KIT
CUI: C0178874
Disease: Tumor Progression
Tumor Progression
0.010 GeneticVariation BEFREE Analysis of a 17-cm malignant GIST in the index patient revealed that it was hemi/homozygous for the germline D820Y mutation, indicating loss of the remaining wild-type KIT allele with tumor progression. 16327443

2005

dbSNP: rs1057519771
rs1057519771
CUI: C0178874
Disease: Tumor Progression
Tumor Progression
0.010 GeneticVariation BEFREE CHMFL-ABL-039 has demonstrated greater efficacies than Imatinib regarding to the anti-proliferation, inhibition of the signaling pathway, arrest of cell cycle progression, induction of apoptosis in vitro and suppression of the tumor progression in vivo in the native and V299L mutated BCR-ABL kinase-driven cells/xenograft models. 30894066

2019

dbSNP: rs1057519847
rs1057519847
CUI: C0178874
Disease: Tumor Progression
Tumor Progression
0.010 GeneticVariation BEFREE Haploinsufficiency of Nkx2-1 enhanced Kras(G12D)-mediated tumor progression, but reduced EGFR(L858R)-mediated progression. 23143308

2012

dbSNP: rs1057519848
rs1057519848
CUI: C0178874
Disease: Tumor Progression
Tumor Progression
0.010 GeneticVariation BEFREE Haploinsufficiency of Nkx2-1 enhanced Kras(G12D)-mediated tumor progression, but reduced EGFR(L858R)-mediated progression. 23143308

2012

dbSNP: rs11549465
rs11549465
CUI: C0178874
Disease: Tumor Progression
Tumor Progression
0.010 GeneticVariation BEFREE Hypoxia-inducible factor-1 (HIF-1) influences cancer progression and metastasis through various mechanisms, and HIF-1α polymorphisms are reportedly associated with many cancers; however, the associations of HIF-1α P582S and A588T polymorphisms with the risk of digestive system cancer remain inconclusive. 24293391

2014

dbSNP: rs11549467
rs11549467
CUI: C0178874
Disease: Tumor Progression
Tumor Progression
0.010 GeneticVariation BEFREE Hypoxia-inducible factor-1 (HIF-1) influences cancer progression and metastasis through various mechanisms, and HIF-1α polymorphisms are reportedly associated with many cancers; however, the associations of HIF-1α P582S and A588T polymorphisms with the risk of digestive system cancer remain inconclusive. 24293391

2014

dbSNP: rs11568818
rs11568818
CUI: C0178874
Disease: Tumor Progression
Tumor Progression
0.010 GeneticVariation BEFREE The -181A→G (rs11568818) polymorphism in the MMP7 promoter modulates gene expression and possibly affects cancer progression. 25847246

2015

dbSNP: rs11672691
rs11672691
CUI: C0178874
Disease: Tumor Progression
Tumor Progression
0.010 GeneticVariation BEFREE We found an association of the aggressive PCa-associated allele G of rs11672691 with elevated transcript levels of two biologically plausible candidate genes, PCAT19 and CEACAM21, implicated in PCa cell growth and tumor progression. 30033361

2018

dbSNP: rs121434568
rs121434568
CUI: C0178874
Disease: Tumor Progression
Tumor Progression
0.010 GeneticVariation BEFREE Haploinsufficiency of Nkx2-1 enhanced Kras(G12D)-mediated tumor progression, but reduced EGFR(L858R)-mediated progression. 23143308

2012

dbSNP: rs121913279
rs121913279
CUI: C0178874
Disease: Tumor Progression
Tumor Progression
0.010 GeneticVariation BEFREE The results suggest PIK3CA H1047R mutant cells have a selective advantage in breast, contribute to breast cancer susceptibility, and drive tumor progression during breast carcinogenesis, even when present as only a subpopulation of tumor cells. 27108388

2016

dbSNP: rs121917887
rs121917887
CUI: C0178874
Disease: Tumor Progression
Tumor Progression
0.010 GeneticVariation BEFREE A similar ser120-gly mutation in NME1 has been found in human neuroblastoma, suggesting that mutation in this region may be a general phenomenon related to tumor progression. 7794272

1995

dbSNP: rs121918464
rs121918464
CUI: C0178874
Disease: Tumor Progression
Tumor Progression
0.010 GeneticVariation BEFREE The E76K GOF mutation is the most common and active SHP2 mutation; however, the pathogenic effects and function of this mutation in CRC tumor progression have not been well characterized. 29323748

2018

dbSNP: rs1273593548
rs1273593548
CUI: C0178874
Disease: Tumor Progression
Tumor Progression
0.010 GeneticVariation BEFREE To determine which KRAS effectors were responsible for tumor progression, we created four effector domain mutants (S35, G37, E38 and C40) in G12V-activated KRAS and expressed these alone or with BrafV600E in mouse lungs... 24489653

2014

dbSNP: rs1285136498
rs1285136498
CUI: C0178874
Disease: Tumor Progression
Tumor Progression
0.010 GeneticVariation BEFREE Besides earlier described DNA methylation, recent studies implicate bone morphogenic protein and non-steroidal anti-inflammatory drugs in control of S100P expression during tumor progression. 20155429

2011

dbSNP: rs1288373809
rs1288373809
CUI: C0178874
Disease: Tumor Progression
Tumor Progression
0.010 GeneticVariation BEFREE Our data showed that (1) the frequency of C609T NQO1 was significantly increased in TNM stage III HCC patients; (2) no significant association was found between p53 expression and C609T polymorphism of NQO1 gene; and (3) a tumor/non-tumor (T/N) ratio > 1.27 of NQO1 expression revealed by real-time qPCR analyses was positively correlated with poorer survival in patients with tumors >5 cm, suggesting that an increase of NQO1 expression may be an indicator of advanced tumor progression. 19688691

2009

dbSNP: rs137852578
rs137852578
AR
CUI: C0178874
Disease: Tumor Progression
Tumor Progression
0.010 GeneticVariation BEFREE Human LNCaP cells, extensively used as a model for androgen-dependent prostate tumor, express the androgen receptor (AR) mutant T877A promiscuously transactivated by estrogens and other ligands, which may further facilitate cancer progression. 12391264

2002

dbSNP: rs1418810723
rs1418810723
FN1
CUI: C0178874
Disease: Tumor Progression
Tumor Progression
0.010 GeneticVariation BEFREE BRAF(V600E) and microenvironment in thyroid cancer: a functional link to drive cancer progression. 21447745

2011

dbSNP: rs1443465532
rs1443465532
CUI: C0178874
Disease: Tumor Progression
Tumor Progression
0.010 GeneticVariation BEFREE These results demonstrate that P125A endostatin inhibits the angiogenic switch during mammary gland adenocarcinoma tumor progression in the C3(1)/Tag transgenic model. 12209972

2002

dbSNP: rs145204276
rs145204276
CUI: C0178874
Disease: Tumor Progression
Tumor Progression
0.010 GeneticVariation BEFREE The allele del of rs145204276 is associated with a remarkably lower incidence of cancer progression and metastasis. 29557411

2018

dbSNP: rs1695
rs1695
CUI: C0178874
Disease: Tumor Progression
Tumor Progression
0.010 GeneticVariation BEFREE The current data, based on a large cohort (n = 929) of Chinese patients with gastric cancer, suggested that the presence of SOD2 rs4880 and GSTP1 rs1695 genotypes may contribute to cancer progression as well as tumor aggressiveness. 22517484

2012

dbSNP: rs17217772
rs17217772
CUI: C0178874
Disease: Tumor Progression
Tumor Progression
0.010 GeneticVariation BEFREE We performed a case-control study to test the association between two polymorphisms in the hMSH2 gene: an A --> G transition at 127 position producing an Asn --> Ser substitution at codon 127 (the Asn127Ser polymorphism) and a G --> A transition at 1032 position resulting in a Gly --> Asp change at codon 322 (the Gly322Asp polymorphism) and breast cancer risk and cancer progression. 16252083

2005