NXN, nucleoredoxin, 64359

N. diseases: 117; N. variants: 7
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1555610590
rs1555610590
Entrez Id: 64359
Gene Symbol: NXN
NXN
CUI: C1840307
Disease:
Distal shortening of limbs 		A 0.700 GeneticVariation CLINVAR
dbSNP: rs73975588
rs73975588
Entrez Id: 64359
Gene Symbol: NXN
NXN
CUI: C0007102
Disease:
Malignant tumor of colon 		A 0.700 GeneticVariation GWASCAT Association analyses identify 31 new risk loci for colorectal cancer susceptibility. 31089142 2019
dbSNP: rs73975588
rs73975588
Entrez Id: 64359
Gene Symbol: NXN
NXN
CUI: C0009402
Disease:
Colorectal Carcinoma 		A 0.700 GeneticVariation GWASCAT Association analyses identify 31 new risk loci for colorectal cancer susceptibility. 31089142 2019
dbSNP: rs73975588
rs73975588
Entrez Id: 64359
Gene Symbol: NXN
NXN
CUI: C2677123
Disease:
COLORECTAL CANCER, SUSCEPTIBILITY TO, 3 		A 0.700 GeneticVariation GWASCAT Association analyses identify 31 new risk loci for colorectal cancer susceptibility. 31089142 2019
dbSNP: rs73975588
rs73975588
Entrez Id: 64359
Gene Symbol: NXN
NXN
CUI: C1837315
Disease:
COLORECTAL CANCER, SUSCEPTIBILITY TO, 1 		A 0.700 GeneticVariation GWASCAT Association analyses identify 31 new risk loci for colorectal cancer susceptibility. 31089142 2019
dbSNP: rs73975588
rs73975588
Entrez Id: 64359
Gene Symbol: NXN
NXN
CUI: C3554460
Disease:
COLORECTAL CANCER, SUSCEPTIBILITY TO, 12 		A 0.700 GeneticVariation GWASCAT Association analyses identify 31 new risk loci for colorectal cancer susceptibility. 31089142 2019
dbSNP: rs73975588
rs73975588
Entrez Id: 64359
Gene Symbol: NXN
NXN
CUI: C0346629
Disease:
Malignant neoplasm of large intestine 		A 0.700 GeneticVariation GWASCAT Association analyses identify 31 new risk loci for colorectal cancer susceptibility. 31089142 2019
dbSNP: rs73975588
rs73975588
Entrez Id: 64359
Gene Symbol: NXN
NXN
CUI: C0009404
Disease:
Colorectal Neoplasms 		A 0.700 GeneticVariation GWASCAT Association analyses identify 31 new risk loci for colorectal cancer susceptibility. 31089142 2019
dbSNP: rs73975588
rs73975588
Entrez Id: 64359
Gene Symbol: NXN
NXN
CUI: C2675481
Disease:
COLORECTAL CANCER, SUSCEPTIBILITY TO, 10 		A 0.700 GeneticVariation GWASCAT Association analyses identify 31 new risk loci for colorectal cancer susceptibility. 31089142 2019
dbSNP: rs73975588
rs73975588
Entrez Id: 64359
Gene Symbol: NXN
NXN
CUI: C1319315
Disease:
Adenocarcinoma of large intestine 		A 0.700 GeneticVariation GWASCAT Association analyses identify 31 new risk loci for colorectal cancer susceptibility. 31089142 2019
dbSNP: rs4968127
rs4968127
Entrez Id: 64359
Gene Symbol: NXN
NXN
CUI: C2675481
Disease:
COLORECTAL CANCER, SUSCEPTIBILITY TO, 10 		G 0.700 GeneticVariation GWASCAT Discovery of common and rare genetic risk variants for colorectal cancer. 30510241 2019
dbSNP: rs4968127
rs4968127
Entrez Id: 64359
Gene Symbol: NXN
NXN
CUI: C3554460
Disease:
COLORECTAL CANCER, SUSCEPTIBILITY TO, 12 		G 0.700 GeneticVariation GWASCAT Discovery of common and rare genetic risk variants for colorectal cancer. 30510241 2019
dbSNP: rs4968127
rs4968127
Entrez Id: 64359
Gene Symbol: NXN
NXN
CUI: C0009404
Disease:
Colorectal Neoplasms 		G 0.700 GeneticVariation GWASCAT Discovery of common and rare genetic risk variants for colorectal cancer. 30510241 2019
dbSNP: rs4968127
rs4968127
Entrez Id: 64359
Gene Symbol: NXN
NXN
CUI: C2677123
Disease:
COLORECTAL CANCER, SUSCEPTIBILITY TO, 3 		G 0.700 GeneticVariation GWASCAT Discovery of common and rare genetic risk variants for colorectal cancer. 30510241 2019
dbSNP: rs4968127
rs4968127
Entrez Id: 64359
Gene Symbol: NXN
NXN
CUI: C0346629
Disease:
Malignant neoplasm of large intestine 		G 0.700 GeneticVariation GWASCAT Discovery of common and rare genetic risk variants for colorectal cancer. 30510241 2019
dbSNP: rs4968127
rs4968127
Entrez Id: 64359
Gene Symbol: NXN
NXN
CUI: C0009402
Disease:
Colorectal Carcinoma 		G 0.700 GeneticVariation GWASCAT Discovery of common and rare genetic risk variants for colorectal cancer. 30510241 2019
dbSNP: rs4968127
rs4968127
Entrez Id: 64359
Gene Symbol: NXN
NXN
CUI: C1837315
Disease:
COLORECTAL CANCER, SUSCEPTIBILITY TO, 1 		G 0.700 GeneticVariation GWASCAT Discovery of common and rare genetic risk variants for colorectal cancer. 30510241 2019
dbSNP: rs4968127
rs4968127
Entrez Id: 64359
Gene Symbol: NXN
NXN
CUI: C1319315
Disease:
Adenocarcinoma of large intestine 		G 0.700 GeneticVariation GWASCAT Discovery of common and rare genetic risk variants for colorectal cancer. 30510241 2019
dbSNP: rs4968127
rs4968127
Entrez Id: 64359
Gene Symbol: NXN
NXN
CUI: C0007102
Disease:
Malignant tumor of colon 		G 0.700 GeneticVariation GWASCAT Discovery of common and rare genetic risk variants for colorectal cancer. 30510241 2019
dbSNP: rs4968127
rs4968127
Entrez Id: 64359
Gene Symbol: NXN
NXN
CUI: C1302401
Disease:
Adenoma of large intestine 		G 0.700 GeneticVariation GWASCAT Discovery of common and rare genetic risk variants for colorectal cancer. 30510241 2019
dbSNP: rs73975586
rs73975586
Entrez Id: 64359;101927727
Gene Symbol: NXN;LOC101927727
NXN;LOC101927727
CUI: C1837315
Disease:
COLORECTAL CANCER, SUSCEPTIBILITY TO, 1 		A 0.700 GeneticVariation GWASCAT Discovery of common and rare genetic risk variants for colorectal cancer. 30510241 2019
dbSNP: rs73975586
rs73975586
Entrez Id: 64359;101927727
Gene Symbol: NXN;LOC101927727
NXN;LOC101927727
CUI: C1319315
Disease:
Adenocarcinoma of large intestine 		A 0.700 GeneticVariation GWASCAT Discovery of common and rare genetic risk variants for colorectal cancer. 30510241 2019
dbSNP: rs73975586
rs73975586
Entrez Id: 64359;101927727
Gene Symbol: NXN;LOC101927727
NXN;LOC101927727
CUI: C0009402
Disease:
Colorectal Carcinoma 		A 0.700 GeneticVariation GWASCAT Discovery of common and rare genetic risk variants for colorectal cancer. 30510241 2019
dbSNP: rs73975586
rs73975586
Entrez Id: 64359;101927727
Gene Symbol: NXN;LOC101927727
NXN;LOC101927727
CUI: C0009404
Disease:
Colorectal Neoplasms 		A 0.700 GeneticVariation GWASCAT Discovery of common and rare genetic risk variants for colorectal cancer. 30510241 2019
dbSNP: rs73975586
rs73975586
Entrez Id: 64359;101927727
Gene Symbol: NXN;LOC101927727
NXN;LOC101927727
CUI: C2677123
Disease:
COLORECTAL CANCER, SUSCEPTIBILITY TO, 3 		A 0.700 GeneticVariation GWASCAT Discovery of common and rare genetic risk variants for colorectal cancer. 30510241 2019