NXN, nucleoredoxin, 64359

N. diseases: 117; N. variants: 7
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs12603526
rs12603526 		0.790 0.080 17 897353 intron variant T/C snv 2.3E-02
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		Digestive System Diseases; Neoplasms 0.800 1.000 2 2014 2016
dbSNP: rs12603526
rs12603526 		0.790 0.080 17 897353 intron variant T/C snv 2.3E-02
CUI: C2675481
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 10
COLORECTAL CANCER, SUSCEPTIBILITY TO, 10 		0.700 1.000 2 2014 2016
dbSNP: rs12603526
rs12603526 		0.790 0.080 17 897353 intron variant T/C snv 2.3E-02
CUI: C1319315
Disease: Adenocarcinoma of large intestine
Adenocarcinoma of large intestine 		Digestive System Diseases; Neoplasms 0.700 1.000 2 2014 2016
dbSNP: rs12603526
rs12603526 		0.790 0.080 17 897353 intron variant T/C snv 2.3E-02
CUI: C2677123
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 3
COLORECTAL CANCER, SUSCEPTIBILITY TO, 3 		0.700 1.000 2 2014 2016
dbSNP: rs12603526
rs12603526 		0.790 0.080 17 897353 intron variant T/C snv 2.3E-02
CUI: C0007102
Disease: Malignant tumor of colon
Malignant tumor of colon 		Digestive System Diseases; Neoplasms 0.700 1.000 2 2014 2016
dbSNP: rs12603526
rs12603526 		0.790 0.080 17 897353 intron variant T/C snv 2.3E-02
CUI: C1837315
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 1
COLORECTAL CANCER, SUSCEPTIBILITY TO, 1 		0.700 1.000 2 2014 2016
dbSNP: rs12603526
rs12603526 		0.790 0.080 17 897353 intron variant T/C snv 2.3E-02
CUI: C0346629
Disease: Malignant neoplasm of large intestine
Malignant neoplasm of large intestine 		Digestive System Diseases; Neoplasms 0.700 1.000 2 2014 2016
dbSNP: rs12603526
rs12603526 		0.790 0.080 17 897353 intron variant T/C snv 2.3E-02
CUI: C3554460
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 12
COLORECTAL CANCER, SUSCEPTIBILITY TO, 12 		0.700 1.000 2 2014 2016
dbSNP: rs12603526
rs12603526 		0.790 0.080 17 897353 intron variant T/C snv 2.3E-02
CUI: C0009404
Disease: Colorectal Neoplasms
Colorectal Neoplasms 		Digestive System Diseases; Neoplasms 0.700 1.000 2 2014 2016
dbSNP: rs4968127
rs4968127 		0.776 0.080 17 906403 intron variant G/A;T snv
CUI: C0007102
Disease: Malignant tumor of colon
Malignant tumor of colon 		Digestive System Diseases; Neoplasms 0.700 1.000 1 2019 2019
dbSNP: rs4968127
rs4968127 		0.776 0.080 17 906403 intron variant G/A;T snv
CUI: C1302401
Disease: Adenoma of large intestine
Adenoma of large intestine 		Digestive System Diseases; Neoplasms 0.700 1.000 1 2019 2019
dbSNP: rs4968127
rs4968127 		0.776 0.080 17 906403 intron variant G/A;T snv
CUI: C2677123
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 3
COLORECTAL CANCER, SUSCEPTIBILITY TO, 3 		0.700 1.000 1 2019 2019
dbSNP: rs4968127
rs4968127 		0.776 0.080 17 906403 intron variant G/A;T snv
CUI: C0009404
Disease: Colorectal Neoplasms
Colorectal Neoplasms 		Digestive System Diseases; Neoplasms 0.700 1.000 1 2019 2019
dbSNP: rs4968127
rs4968127 		0.776 0.080 17 906403 intron variant G/A;T snv
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		Digestive System Diseases; Neoplasms 0.700 1.000 1 2019 2019
dbSNP: rs4968127
rs4968127 		0.776 0.080 17 906403 intron variant G/A;T snv
CUI: C1319315
Disease: Adenocarcinoma of large intestine
Adenocarcinoma of large intestine 		Digestive System Diseases; Neoplasms 0.700 1.000 1 2019 2019
dbSNP: rs4968127
rs4968127 		0.776 0.080 17 906403 intron variant G/A;T snv
CUI: C3554460
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 12
COLORECTAL CANCER, SUSCEPTIBILITY TO, 12 		0.700 1.000 1 2019 2019
dbSNP: rs4968127
rs4968127 		0.776 0.080 17 906403 intron variant G/A;T snv
CUI: C0346629
Disease: Malignant neoplasm of large intestine
Malignant neoplasm of large intestine 		Digestive System Diseases; Neoplasms 0.700 1.000 1 2019 2019
dbSNP: rs4968127
rs4968127 		0.776 0.080 17 906403 intron variant G/A;T snv
CUI: C1837315
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 1
COLORECTAL CANCER, SUSCEPTIBILITY TO, 1 		0.700 1.000 1 2019 2019
dbSNP: rs4968127
rs4968127 		0.776 0.080 17 906403 intron variant G/A;T snv
CUI: C2675481
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 10
COLORECTAL CANCER, SUSCEPTIBILITY TO, 10 		0.700 1.000 1 2019 2019
dbSNP: rs73975586
rs73975586 		0.776 0.080 17 911003 non coding transcript exon variant A/T snv 9.8E-02
CUI: C2677123
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 3
COLORECTAL CANCER, SUSCEPTIBILITY TO, 3 		0.700 1.000 1 2019 2019
dbSNP: rs73975586
rs73975586 		0.776 0.080 17 911003 non coding transcript exon variant A/T snv 9.8E-02
CUI: C0007102
Disease: Malignant tumor of colon
Malignant tumor of colon 		Digestive System Diseases; Neoplasms 0.700 1.000 1 2019 2019
dbSNP: rs73975586
rs73975586 		0.776 0.080 17 911003 non coding transcript exon variant A/T snv 9.8E-02
CUI: C0009404
Disease: Colorectal Neoplasms
Colorectal Neoplasms 		Digestive System Diseases; Neoplasms 0.700 1.000 1 2019 2019
dbSNP: rs73975586
rs73975586 		0.776 0.080 17 911003 non coding transcript exon variant A/T snv 9.8E-02
CUI: C3554460
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 12
COLORECTAL CANCER, SUSCEPTIBILITY TO, 12 		0.700 1.000 1 2019 2019
dbSNP: rs73975586
rs73975586 		0.776 0.080 17 911003 non coding transcript exon variant A/T snv 9.8E-02
CUI: C1319315
Disease: Adenocarcinoma of large intestine
Adenocarcinoma of large intestine 		Digestive System Diseases; Neoplasms 0.700 1.000 1 2019 2019
dbSNP: rs73975586
rs73975586 		0.776 0.080 17 911003 non coding transcript exon variant A/T snv 9.8E-02
CUI: C1302401
Disease: Adenoma of large intestine
Adenoma of large intestine 		Digestive System Diseases; Neoplasms 0.700 1.000 1 2019 2019