Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2273535
rs2273535
CUI: C0178874
Disease: Tumor Progression
Tumor Progression
0.020 GeneticVariation BEFREE For esophageal cancer, the AurkA Phe31-Ile polymorphism has previously been associated with tumor progression. 29560108

2018

dbSNP: rs1284806277
rs1284806277
MOK
CUI: C0178874
Disease: Tumor Progression
Tumor Progression
0.020 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: rs1284806277
rs1284806277
MOK
CUI: C0178874
Disease: Tumor Progression
Tumor Progression
0.020 GeneticVariation BEFREE Stable S100P knockdown CRC cell lines were established to elucidate the relationship between S100P expression and tumor progression in vitro and in vivo. 26975699

2016

dbSNP: rs969139366
rs969139366
CUI: C0178874
Disease: Tumor Progression
Tumor Progression
0.010 GeneticVariation BEFREE It was worth noting that 31 inhibited GIST-T1 tumor growth (TGI = 81.5%) and even the BaF3-TEL-cKIT-T670I tumor progression (TGI = 41.9%, 1-resistant GISTs) at a dosage of 100 mg/kg/day without exhibiting apparent toxicity. 28541695

2017

dbSNP: rs961150162
rs961150162
CUI: C0178874
Disease: Tumor Progression
Tumor Progression
0.010 GeneticVariation BEFREE The DDR2 E655K mutation can play a role in cancer progression by reducing the growth-inhibitory effect of collagen. 26826182

2016

dbSNP: rs9282861
rs9282861
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: rs869320694
rs869320694
CUI: C0178874
Disease: Tumor Progression
Tumor Progression
0.010 GeneticVariation BEFREE The DDR2 E655K mutation can play a role in cancer progression by reducing the growth-inhibitory effect of collagen. 26826182

2016

dbSNP: rs773862672
rs773862672
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: rs77375493
rs77375493
CUI: C0178874
Disease: Tumor Progression
Tumor Progression
0.010 GeneticVariation BEFREE A role for reactive oxygen species in JAK2 V617F myeloproliferative neoplasm progression. 23558526

2013

dbSNP: rs767808984
rs767808984
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: rs762807774
rs762807774
CUI: C0178874
Disease: Tumor Progression
Tumor Progression
0.010 GeneticVariation BEFREE Mutated MITF-E87R in Melanoma Enhances Tumor Progression via S100A4. 29679610

2018

dbSNP: rs727503094
rs727503094
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: rs720012
rs720012
CUI: C0178874
Disease: Tumor Progression
Tumor Progression
0.010 GeneticVariation BEFREE Two linked SNPs (rs2073778 and rs720012) in DGCR8 showed significant association with tumor progression (HR = 4.00, 95% CI = 1.53-10.46, P = 0.005). 23322153

2013

dbSNP: rs7121
rs7121
CUI: C0178874
Disease: Tumor Progression
Tumor Progression
0.010 GeneticVariation BEFREE In this review and meta-analysis, we focus on the synonymous SNP rs7121 (<i>FokI</i>, c.393C>T), which is associated with either tumor progression or prolonged survival in cancer patients (overall hazard ratio = 2.256; p < 0.001). 31124412

2019

dbSNP: rs587782529
rs587782529
CUI: C0178874
Disease: Tumor Progression
Tumor Progression
0.010 GeneticVariation BEFREE Thus, the R337C mutant retains some functional activity yet leads to a predisposition to cancer, suggesting that even partial inactivation of p53 oligomerization is sufficient for accelerated tumour progression. 9704931

1998

dbSNP: rs587782148
rs587782148
CUI: C0178874
Disease: Tumor Progression
Tumor Progression
0.010 GeneticVariation BEFREE Sequencing of margins with dysplasia demonstrated an identical nonconservative mitochondrial mutation (A76T in ND4L) as the tumor, suggesting a role of mtDNA mutation in tumor progression. 17456604

2007

dbSNP: rs562015640
rs562015640
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: rs55958994
rs55958994
CUI: C0178874
Disease: Tumor Progression
Tumor Progression
0.010 GeneticVariation BEFREE The prostate cancer risk variant rs55958994 regulates multiple gene expression through extreme long-range chromatin interaction to control tumor progression. 31328168

2019

dbSNP: rs557263543
rs557263543
CUI: C0178874
Disease: Tumor Progression
Tumor Progression
0.010 GeneticVariation BEFREE The DDR2 E655K mutation can play a role in cancer progression by reducing the growth-inhibitory effect of collagen. 26826182

2016

dbSNP: rs4987188
rs4987188
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

dbSNP: rs4986791
rs4986791
CUI: C0178874
Disease: Tumor Progression
Tumor Progression
0.010 GeneticVariation BEFREE Caco-2 cells that expressed TLR4-D299G underwent the epithelial-mesenchymal transition and morphologic changes associated with tumor progression, whereas cells that expressed wild-type TLR4 or TLR4-T399I did not. 21920464

2011

dbSNP: rs4986790
rs4986790
CUI: C0178874
Disease: Tumor Progression
Tumor Progression
0.010 GeneticVariation BEFREE TLR4-D299G induces features of neoplastic progression in intestinal epithelial Caco-2 cells and associates with aggressive colon cancer in humans, implying a novel link between aberrant innate immunity and colonic cancerogenesis. 21920464

2011

dbSNP: rs4880
rs4880
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: rs4444235
rs4444235
CUI: C0178874
Disease: Tumor Progression
Tumor Progression
0.010 GeneticVariation BEFREE LOH analysis suggested that the three CRC risk variants, rs12657484, rs3802842, and rs4444235, exhibited somatic allele-specific imbalance and might be critical during neoplastic progression. 24968322

2014

dbSNP: rs438034
rs438034
CUI: C0178874
Disease: Tumor Progression
Tumor Progression
0.010 GeneticVariation BEFREE In addition, the 52 single nucleotide polymorphisms associated at P<10(-4) included rs438034 (CENPF; P=4.86×10(-6)), previously correlated with cancer progression, and rs2255235 (B2M; P=3.10×10(-5)) and rs2064501 (IL22RA2; P=4.81×10(-5)) which map to B-cell genes. 21659360

2011