rs4444235, None

N. diseases: 23
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
1962 0.701 0.240 14 53944201 downstream gene variant T/C snv 0.43 0.900 1.000 14 2008 2019
Malignant tumor of colon
CUI: C0007102
Disease: Malignant tumor of colon
688 0.701 0.240 14 53944201 downstream gene variant T/C snv 0.43 0.710 1.000 4 2008 2019
Adenocarcinoma of large intestine
CUI: C1319315
Disease: Adenocarcinoma of large intestine
432 0.701 0.240 14 53944201 downstream gene variant T/C snv 0.43 0.700 1.000 3 2008 2019
COLORECTAL CANCER, SUSCEPTIBILITY TO, 1
374 0.701 0.240 14 53944201 downstream gene variant T/C snv 0.43 0.700 1.000 3 2008 2019
COLORECTAL CANCER, SUSCEPTIBILITY TO, 10
370 0.701 0.240 14 53944201 downstream gene variant T/C snv 0.43 0.700 1.000 3 2008 2019
COLORECTAL CANCER, SUSCEPTIBILITY TO, 12
373 0.701 0.240 14 53944201 downstream gene variant T/C snv 0.43 0.700 1.000 3 2008 2019
COLORECTAL CANCER, SUSCEPTIBILITY TO, 3
368 0.701 0.240 14 53944201 downstream gene variant T/C snv 0.43 0.700 1.000 3 2008 2019
Colorectal Neoplasms
CUI: C0009404
Disease: Colorectal Neoplasms
609 0.701 0.240 14 53944201 downstream gene variant T/C snv 0.43 0.700 1.000 3 2008 2019
Malignant neoplasm of large intestine
375 0.701 0.240 14 53944201 downstream gene variant T/C snv 0.43 0.700 1.000 3 2008 2019
Nasopharyngeal carcinoma
CUI: C2931822
Disease: Nasopharyngeal carcinoma
320 0.701 0.240 14 53944201 downstream gene variant T/C snv 0.43 0.700 1.000 1 2010 2010
Malignant neoplasm of colon and/or rectum
502 0.701 0.240 14 53944201 downstream gene variant T/C snv 0.43 0.050 1.000 5 2012 2019
Adenoma of large intestine
CUI: C1302401
Disease: Adenoma of large intestine
213 0.701 0.240 14 53944201 downstream gene variant T/C snv 0.43 0.010 1.000 1 2015 2015
Alcohol or Other Drugs use
CUI: C0237123
Disease: Alcohol or Other Drugs use
21 0.701 0.240 14 53944201 downstream gene variant T/C snv 0.43 0.010 1.000 1 2012 2012
Carcinogenesis
CUI: C0596263
Disease: Carcinogenesis
355 0.701 0.240 14 53944201 downstream gene variant T/C snv 0.43 0.010 1.000 1 2019 2019
Colon Carcinoma
CUI: C0699790
Disease: Colon Carcinoma
275 0.701 0.240 14 53944201 downstream gene variant T/C snv 0.43 0.010 1.000 1 2013 2013
Colonic Diseases
CUI: C0009373
Disease: Colonic Diseases
8 0.701 0.240 14 53944201 downstream gene variant T/C snv 0.43 0.010 1.000 1 2012 2012
Esophageal carcinoma
CUI: C0152018
Disease: Esophageal carcinoma
272 0.701 0.240 14 53944201 downstream gene variant T/C snv 0.43 0.010 1.000 1 2015 2015
Esophageal Neoplasms
CUI: C0014859
Disease: Esophageal Neoplasms
270 0.701 0.240 14 53944201 downstream gene variant T/C snv 0.43 0.010 1.000 1 2015 2015
Hereditary Nonpolyposis Colorectal Cancer
1331 0.701 0.240 14 53944201 downstream gene variant T/C snv 0.43 0.010 1.000 1 2012 2012
Lynch Syndrome
CUI: C4552100
Disease: Lynch Syndrome
65 0.701 0.240 14 53944201 downstream gene variant T/C snv 0.43 0.010 1.000 1 2012 2012
Malignant neoplasm of esophagus
CUI: C0546837
Disease: Malignant neoplasm of esophagus
214 0.701 0.240 14 53944201 downstream gene variant T/C snv 0.43 0.010 1.000 1 2015 2015
Neoplasms
CUI: C0027651
Disease: Neoplasms
1644 0.701 0.240 14 53944201 downstream gene variant T/C snv 0.43 0.010 1.000 1 2012 2012
Tumor Progression
CUI: C0178874
Disease: Tumor Progression
72 0.701 0.240 14 53944201 downstream gene variant T/C snv 0.43 0.010 1.000 1 2014 2014