rs11556218, IL16

N. diseases: 27
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.
Primary biliary cirrhosis
CUI: C0008312
Disease: Primary biliary cirrhosis
667 0.653 0.600 15 81305928 missense variant T/G snv 9.6E-02 0.12 0.700 1.000 1 2017 2017
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
1962 0.653 0.600 15 81305928 missense variant T/G snv 9.6E-02 0.12 0.030 1.000 3 2009 2014
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.653 0.600 15 81305928 missense variant T/G snv 9.6E-02 0.12 0.030 1.000 3 2011 2013
Nasopharyngeal carcinoma
CUI: C2931822
Disease: Nasopharyngeal carcinoma
320 0.653 0.600 15 81305928 missense variant T/G snv 9.6E-02 0.12 0.030 1.000 3 2009 2014
Endometriosis
CUI: C0014175
Disease: Endometriosis
274 0.653 0.600 15 81305928 missense variant T/G snv 9.6E-02 0.12 0.020 0.500 2 2010 2018
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1641 0.653 0.600 15 81305928 missense variant T/G snv 9.6E-02 0.12 0.020 1.000 2 2014 2014
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
1374 0.653 0.600 15 81305928 missense variant T/G snv 9.6E-02 0.12 0.020 1.000 2 2014 2014
Renal Cell Carcinoma
CUI: C0007134
Disease: Renal Cell Carcinoma
288 0.653 0.600 15 81305928 missense variant T/G snv 9.6E-02 0.12 0.020 0.500 2 2016 2019
Childhood Osteosarcoma
CUI: C1332986
Disease: Childhood Osteosarcoma
151 0.653 0.600 15 81305928 missense variant T/G snv 9.6E-02 0.12 0.010 1.000 1 2016 2016
Conventional (Clear Cell) Renal Cell Carcinoma
222 0.653 0.600 15 81305928 missense variant T/G snv 9.6E-02 0.12 0.010 1 2019 2019
Coronary Arteriosclerosis
CUI: C0010054
Disease: Coronary Arteriosclerosis
440 0.653 0.600 15 81305928 missense variant T/G snv 9.6E-02 0.12 0.010 1.000 1 2011 2011
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.653 0.600 15 81305928 missense variant T/G snv 9.6E-02 0.12 0.010 1.000 1 2011 2011
Diabetes Mellitus, Non-Insulin-Dependent
2672 0.653 0.600 15 81305928 missense variant T/G snv 9.6E-02 0.12 0.010 1.000 1 2019 2019
Hepatitis B, Chronic
CUI: C0524909
Disease: Hepatitis B, Chronic
84 0.653 0.600 15 81305928 missense variant T/G snv 9.6E-02 0.12 0.010 1.000 1 2011 2011
Liver carcinoma
CUI: C2239176
Disease: Liver carcinoma
942 0.653 0.600 15 81305928 missense variant T/G snv 9.6E-02 0.12 0.010 1.000 1 2011 2011
Lupus Erythematosus, Systemic
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
1172 0.653 0.600 15 81305928 missense variant T/G snv 9.6E-02 0.12 0.010 1.000 1 2009 2009
Malignant neoplasm of colon and/or rectum
502 0.653 0.600 15 81305928 missense variant T/G snv 9.6E-02 0.12 0.010 1.000 1 2014 2014
Malignant neoplasm of prostate
CUI: C0376358
Disease: Malignant neoplasm of prostate
1082 0.653 0.600 15 81305928 missense variant T/G snv 9.6E-02 0.12 0.010 1.000 1 2012 2012
Malignant neoplasm of stomach
CUI: C0024623
Disease: Malignant neoplasm of stomach
615 0.653 0.600 15 81305928 missense variant T/G snv 9.6E-02 0.12 0.010 1.000 1 2013 2013
Multiple Sclerosis
CUI: C0026769
Disease: Multiple Sclerosis
1022 0.653 0.600 15 81305928 missense variant T/G snv 9.6E-02 0.12 0.010 1.000 1 2017 2017
Osteoarthritis, Knee
CUI: C0409959
Disease: Osteoarthritis, Knee
150 0.653 0.600 15 81305928 missense variant T/G snv 9.6E-02 0.12 0.010 1.000 1 2015 2015
Osteoporosis
CUI: C0029456
Disease: Osteoporosis
182 0.653 0.600 15 81305928 missense variant T/G snv 9.6E-02 0.12 0.010 1.000 1 2017 2017
Osteosarcoma
CUI: C0029463
Disease: Osteosarcoma
178 0.653 0.600 15 81305928 missense variant T/G snv 9.6E-02 0.12 0.010 1.000 1 2016 2016
Osteosarcoma of bone
CUI: C0585442
Disease: Osteosarcoma of bone
151 0.653 0.600 15 81305928 missense variant T/G snv 9.6E-02 0.12 0.010 1.000 1 2016 2016
Pancreatitis
CUI: C0030305
Disease: Pancreatitis
80 0.653 0.600 15 81305928 missense variant T/G snv 9.6E-02 0.12 0.010 1.000 1 2017 2017