Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs753665559
rs753665559
Entrez Id: 6416
Gene Symbol: MAP2K4
MAP2K4
CUI: C1319315
Disease:
Adenocarcinoma of large intestine
0.700 GeneticVariation UNIPROT
dbSNP: rs3826392
rs3826392
Entrez Id: 6416;7566
Gene Symbol: MAP2K4;ZNF18
MAP2K4;ZNF18
CUI: C0948008
Disease:
Ischemic stroke
0.010 GeneticVariation BEFREE This result suggests that rs3826392 may play a potential role in the IS inflammatory process. 26856463 2016
dbSNP: rs12939944
rs12939944
Entrez Id: 6416
Gene Symbol: MAP2K4
MAP2K4
CUI: C0346647
Disease:
Malignant neoplasm of pancreas
0.010 GeneticVariation BEFREE Using an approach based on candidate genes whose roles in pancreatic cancer have been well known, we identified two new susceptibility loci. rs11571836 located in the BRCA2 3'-untranslated region was significantly associated with lower expression of BRCA2 transcript and increased pancreatic cancer risk [odds ratio = 1.30, 95% confidence interval = 1.14-1.47, P = 7.64 × 10(-5)] in a recessive manner. rs12939944 located in the MAP2K4 intron was associated with decreased risk (odds ratio = 0.82, 95% confidence interval = 0.74-0.91, P = 0.0001) in a dominant manner. 23299404 2013
dbSNP: rs12939944
rs12939944
Entrez Id: 6416
Gene Symbol: MAP2K4
MAP2K4
CUI: C0235974
Disease:
Pancreatic carcinoma
0.010 GeneticVariation BEFREE Using an approach based on candidate genes whose roles in pancreatic cancer have been well known, we identified two new susceptibility loci. rs11571836 located in the BRCA2 3'-untranslated region was significantly associated with lower expression of BRCA2 transcript and increased pancreatic cancer risk [odds ratio = 1.30, 95% confidence interval = 1.14-1.47, P = 7.64 × 10(-5)] in a recessive manner. rs12939944 located in the MAP2K4 intron was associated with decreased risk (odds ratio = 0.82, 95% confidence interval = 0.74-0.91, P = 0.0001) in a dominant manner. 23299404 2013
dbSNP: rs3809728
rs3809728
Entrez Id: 6416;7566
Gene Symbol: MAP2K4;ZNF18
MAP2K4;ZNF18
CUI: C0302592
Disease:
Cervix carcinoma
0.010 GeneticVariation BEFREE In the current, hospital-based case-control study of 471 cervical cancer cases and 600 sex and age frequency-matched cancer-free controls in an Eastern Chinese population, we genotyped two common polymorphisms in the MKK4 promoter region (-1304T>G, rs3826392 and -1044A>T, rs3809728)c and assessed their associations with the risk of cervical cancer. 22335172 2012
dbSNP: rs3809728
rs3809728
Entrez Id: 6416;7566
Gene Symbol: MAP2K4;ZNF18
MAP2K4;ZNF18
CUI: C4048328
Disease:
cervical cancer
0.010 GeneticVariation BEFREE In the current, hospital-based case-control study of 471 cervical cancer cases and 600 sex and age frequency-matched cancer-free controls in an Eastern Chinese population, we genotyped two common polymorphisms in the MKK4 promoter region (-1304T>G, rs3826392 and -1044A>T, rs3809728)c and assessed their associations with the risk of cervical cancer. 22335172 2012
dbSNP: rs3809728
rs3809728
Entrez Id: 6416;7566
Gene Symbol: MAP2K4;ZNF18
MAP2K4;ZNF18
CUI: C0007847
Disease:
Malignant tumor of cervix
0.010 GeneticVariation BEFREE In the current, hospital-based case-control study of 471 cervical cancer cases and 600 sex and age frequency-matched cancer-free controls in an Eastern Chinese population, we genotyped two common polymorphisms in the MKK4 promoter region (-1304T>G, rs3826392 and -1044A>T, rs3809728)c and assessed their associations with the risk of cervical cancer. 22335172 2012
dbSNP: rs3826392
rs3826392
Entrez Id: 6416;7566
Gene Symbol: MAP2K4;ZNF18
MAP2K4;ZNF18
CUI: C4048328
Disease:
cervical cancer
0.010 GeneticVariation BEFREE In the current, hospital-based case-control study of 471 cervical cancer cases and 600 sex and age frequency-matched cancer-free controls in an Eastern Chinese population, we genotyped two common polymorphisms in the MKK4 promoter region (-1304T>G, rs3826392 and -1044A>T, rs3809728)c and assessed their associations with the risk of cervical cancer. 22335172 2012
dbSNP: rs3826392
rs3826392
Entrez Id: 6416;7566
Gene Symbol: MAP2K4;ZNF18
MAP2K4;ZNF18
CUI: C0007847
Disease:
Malignant tumor of cervix
0.010 GeneticVariation BEFREE In the current, hospital-based case-control study of 471 cervical cancer cases and 600 sex and age frequency-matched cancer-free controls in an Eastern Chinese population, we genotyped two common polymorphisms in the MKK4 promoter region (-1304T>G, rs3826392 and -1044A>T, rs3809728)c and assessed their associations with the risk of cervical cancer. 22335172 2012
dbSNP: rs3826392
rs3826392
Entrez Id: 6416;7566
Gene Symbol: MAP2K4;ZNF18
MAP2K4;ZNF18
CUI: C0302592
Disease:
Cervix carcinoma
0.010 GeneticVariation BEFREE In the current, hospital-based case-control study of 471 cervical cancer cases and 600 sex and age frequency-matched cancer-free controls in an Eastern Chinese population, we genotyped two common polymorphisms in the MKK4 promoter region (-1304T>G, rs3826392 and -1044A>T, rs3809728)c and assessed their associations with the risk of cervical cancer. 22335172 2012
dbSNP: rs3809728
rs3809728
Entrez Id: 6416;7566
Gene Symbol: MAP2K4;ZNF18
MAP2K4;ZNF18
CUI: C0009402
Disease:
Colorectal Carcinoma
0.010 GeneticVariation BEFREE In current hospital-based case-control study of 706 patients with sporadic colorectal cancer (CRC) and 723 sex-age-frequency-matched control subjects in a southern Chinese population, we genotyped two polymorphisms of MKK4 promoter (i.e., -1304T>G, rs3826392 and -1044A>T, rs3809728) and assessed their associations with the risk of sporadic CRC. 19610067 2009
dbSNP: rs3826392
rs3826392
Entrez Id: 6416;7566
Gene Symbol: MAP2K4;ZNF18
MAP2K4;ZNF18
CUI: C0009402
Disease:
Colorectal Carcinoma
0.010 GeneticVariation BEFREE In current hospital-based case-control study of 706 patients with sporadic colorectal cancer (CRC) and 723 sex-age-frequency-matched control subjects in a southern Chinese population, we genotyped two polymorphisms of MKK4 promoter (i.e., -1304T>G, rs3826392 and -1044A>T, rs3809728) and assessed their associations with the risk of sporadic CRC. 19610067 2009