rs4778889, IL16

N. diseases: 24
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 0.683 0.480 15 81296654 intron variant T/C snv 0.24 0.030 0.333 3 2014 2014
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
1374 0.683 0.480 15 81296654 intron variant T/C snv 0.24 0.030 0.333 3 2014 2014
Renal Cell Carcinoma
CUI: C0007134
Disease: Renal Cell Carcinoma
288 0.683 0.480 15 81296654 intron variant T/C snv 0.24 0.030 0.667 3 2015 2019
Childhood Renal Cell Carcinoma
CUI: C1333001
Disease: Childhood Renal Cell Carcinoma
10 0.683 0.480 15 81296654 intron variant T/C snv 0.24 0.020 1.000 2 2015 2016
Malignant neoplasm of kidney
CUI: C0740457
Disease: Malignant neoplasm of kidney
22 0.683 0.480 15 81296654 intron variant T/C snv 0.24 0.020 1.000 2 2015 2016
Childhood Osteosarcoma
CUI: C1332986
Disease: Childhood Osteosarcoma
151 0.683 0.480 15 81296654 intron variant T/C snv 0.24 0.010 1 2016 2016
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
1962 0.683 0.480 15 81296654 intron variant T/C snv 0.24 0.010 1.000 1 2011 2011
Conventional (Clear Cell) Renal Cell Carcinoma
CUI: C0279702
Disease: Conventional (Clear Cell) Renal Cell Carcinoma
222 0.683 0.480 15 81296654 intron variant T/C snv 0.24 0.010 1 2019 2019
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.683 0.480 15 81296654 intron variant T/C snv 0.24 0.010 1.000 1 2011 2011
Diabetes
CUI: C0011847
Disease: Diabetes
710 0.683 0.480 15 81296654 intron variant T/C snv 0.24 0.010 1.000 1 2015 2015
Diabetes Mellitus
CUI: C0011849
Disease: Diabetes Mellitus
824 0.683 0.480 15 81296654 intron variant T/C snv 0.24 0.010 1.000 1 2015 2015
Diabetes Mellitus, Non-Insulin-Dependent
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
2672 0.683 0.480 15 81296654 intron variant T/C snv 0.24 0.010 1 2019 2019
Endometriosis
CUI: C0014175
Disease: Endometriosis
274 0.683 0.480 15 81296654 intron variant T/C snv 0.24 0.010 1.000 1 2010 2010
Graves Disease
CUI: C0018213
Disease: Graves Disease
352 0.683 0.480 15 81296654 intron variant T/C snv 0.24 0.010 1.000 1 2008 2008
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
1085 0.683 0.480 15 81296654 intron variant T/C snv 0.24 0.010 1.000 1 2015 2015
Liver carcinoma
CUI: C2239176
Disease: Liver carcinoma
942 0.683 0.480 15 81296654 intron variant T/C snv 0.24 0.010 1.000 1 2011 2011
Lupus Erythematosus, Systemic
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
1172 0.683 0.480 15 81296654 intron variant T/C snv 0.24 0.010 1.000 1 2009 2009
Malignant neoplasm of stomach
CUI: C0024623
Disease: Malignant neoplasm of stomach
615 0.683 0.480 15 81296654 intron variant T/C snv 0.24 0.010 1.000 1 2013 2013
Multiple Sclerosis
CUI: C0026769
Disease: Multiple Sclerosis
1022 0.683 0.480 15 81296654 intron variant T/C snv 0.24 0.010 1.000 1 2017 2017
Osteoarthritis, Knee
CUI: C0409959
Disease: Osteoarthritis, Knee
150 0.683 0.480 15 81296654 intron variant T/C snv 0.24 0.010 1.000 1 2015 2015
Osteosarcoma
CUI: C0029463
Disease: Osteosarcoma
178 0.683 0.480 15 81296654 intron variant T/C snv 0.24 0.010 1 2016 2016
Osteosarcoma of bone
CUI: C0585442
Disease: Osteosarcoma of bone
151 0.683 0.480 15 81296654 intron variant T/C snv 0.24 0.010 1 2016 2016
Pain
CUI: C0030193
Disease: Pain
196 0.683 0.480 15 81296654 intron variant T/C snv 0.24 0.010 1.000 1 2010 2010
Stomach Carcinoma
CUI: C0699791
Disease: Stomach Carcinoma
652 0.683 0.480 15 81296654 intron variant T/C snv 0.24 0.010 1.000 1 2013 2013