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.
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1641 0.574 0.680 11 111511840 intron variant T/C snv 0.32 0.100 0.846 13 2014 2019
Liver carcinoma
CUI: C2239176
Disease: Liver carcinoma
942 0.574 0.680 11 111511840 intron variant T/C snv 0.32 0.100 0.750 12 2011 2018
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
1374 0.574 0.680 11 111511840 intron variant T/C snv 0.32 0.100 0.833 12 2014 2019
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
1962 0.574 0.680 11 111511840 intron variant T/C snv 0.32 0.070 0.857 7 2013 2019
Squamous cell carcinoma of esophagus
329 0.574 0.680 11 111511840 intron variant T/C snv 0.32 0.060 1.000 6 2013 2019
Malignant neoplasm of colon and/or rectum
502 0.574 0.680 11 111511840 intron variant T/C snv 0.32 0.040 0.750 4 2014 2018
Malignant neoplasm of stomach
CUI: C0024623
Disease: Malignant neoplasm of stomach
615 0.574 0.680 11 111511840 intron variant T/C snv 0.32 0.040 0.750 4 2014 2019
Stomach Carcinoma
CUI: C0699791
Disease: Stomach Carcinoma
652 0.574 0.680 11 111511840 intron variant T/C snv 0.32 0.040 0.750 4 2014 2019
Acute lymphocytic leukemia
CUI: C0023449
Disease: Acute lymphocytic leukemia
222 0.574 0.680 11 111511840 intron variant T/C snv 0.32 0.030 1.000 3 2016 2019
Adult Hepatocellular Carcinoma
CUI: C0279607
Disease: Adult Hepatocellular Carcinoma
14 0.574 0.680 11 111511840 intron variant T/C snv 0.32 0.020 0.500 2 2014 2015
Breast Carcinoma
CUI: C0678222
Disease: Breast Carcinoma
2793 0.574 0.680 11 111511840 intron variant T/C snv 0.32 0.020 1.000 2 2013 2014
Carcinogenesis
CUI: C0596263
Disease: Carcinogenesis
355 0.574 0.680 11 111511840 intron variant T/C snv 0.32 0.020 1.000 2 2016 2017
Central neuroblastoma
CUI: C0700095
Disease: Central neuroblastoma
231 0.574 0.680 11 111511840 intron variant T/C snv 0.32 0.020 1.000 2 2019 2019
Childhood Acute Lymphoblastic Leukemia
261 0.574 0.680 11 111511840 intron variant T/C snv 0.32 0.020 1.000 2 2016 2016
Childhood Hepatocellular Carcinoma
CUI: C0279606
Disease: Childhood Hepatocellular Carcinoma
17 0.574 0.680 11 111511840 intron variant T/C snv 0.32 0.020 0.500 2 2014 2015
Childhood Neuroblastoma
CUI: C4086165
Disease: Childhood Neuroblastoma
231 0.574 0.680 11 111511840 intron variant T/C snv 0.32 0.020 1.000 2 2019 2019
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.574 0.680 11 111511840 intron variant T/C snv 0.32 0.020 0.500 2 2013 2019
Esophageal carcinoma
CUI: C0152018
Disease: Esophageal carcinoma
272 0.574 0.680 11 111511840 intron variant T/C snv 0.32 0.020 1.000 2 2013 2018
Esophageal Neoplasms
CUI: C0014859
Disease: Esophageal Neoplasms
270 0.574 0.680 11 111511840 intron variant T/C snv 0.32 0.020 1.000 2 2013 2018
Malignant neoplasm of breast
CUI: C0006142
Disease: Malignant neoplasm of breast
3417 0.574 0.680 11 111511840 intron variant T/C snv 0.32 0.020 1.000 2 2013 2014
Malignant neoplasm of esophagus
CUI: C0546837
Disease: Malignant neoplasm of esophagus
214 0.574 0.680 11 111511840 intron variant T/C snv 0.32 0.020 1.000 2 2013 2018
Malignant neoplasm of gastrointestinal tract
55 0.574 0.680 11 111511840 intron variant T/C snv 0.32 0.020 1.000 2 2015 2019
Malignant neoplasm of liver
CUI: C0345904
Disease: Malignant neoplasm of liver
88 0.574 0.680 11 111511840 intron variant T/C snv 0.32 0.020 0.500 2 2014 2015
Malignant neoplasm of prostate
CUI: C0376358
Disease: Malignant neoplasm of prostate
1082 0.574 0.680 11 111511840 intron variant T/C snv 0.32 0.020 1.000 2 2017 2019
Nasopharyngeal carcinoma
CUI: C2931822
Disease: Nasopharyngeal carcinoma
320 0.574 0.680 11 111511840 intron variant T/C snv 0.32 0.020 1.000 2 2013 2014