Source: BEFREE

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs4778889
rs4778889
IL16
0.683 0.480 15 81296654 intron variant T/C snv 0.24
CUI: C0007134
Disease: Renal Cell Carcinoma
Renal Cell Carcinoma 		0.030 0.667 3 2015 2019
dbSNP: rs4778889
rs4778889
IL16
0.683 0.480 15 81296654 intron variant T/C snv 0.24
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms 		0.030 0.333 3 2014 2014
dbSNP: rs4778889
rs4778889
IL16
0.683 0.480 15 81296654 intron variant T/C snv 0.24
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm 		0.030 0.333 3 2014 2014
dbSNP: rs4778889
rs4778889
IL16
0.683 0.480 15 81296654 intron variant T/C snv 0.24
CUI: C0740457
Disease: Malignant neoplasm of kidney
Malignant neoplasm of kidney 		0.020 1.000 2 2015 2016
dbSNP: rs4778889
rs4778889
IL16
0.683 0.480 15 81296654 intron variant T/C snv 0.24
CUI: C1333001
Disease: Childhood Renal Cell Carcinoma
Childhood Renal Cell Carcinoma 		0.020 1.000 2 2015 2016
dbSNP: rs4778889
rs4778889
IL16
0.683 0.480 15 81296654 intron variant T/C snv 0.24
CUI: C0279702
Disease: Conventional (Clear Cell) Renal Cell Carcinoma
Conventional (Clear Cell) Renal Cell Carcinoma 		0.010 < 0.001 1 2019 2019
dbSNP: rs4778889
rs4778889
IL16
0.683 0.480 15 81296654 intron variant T/C snv 0.24
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		0.010 < 0.001 1 2019 2019
dbSNP: rs4778889
rs4778889
IL16
0.683 0.480 15 81296654 intron variant T/C snv 0.24
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		0.010 1.000 1 2017 2017
dbSNP: rs4778889
rs4778889
IL16
0.683 0.480 15 81296654 intron variant T/C snv 0.24
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma 		0.010 1.000 1 2013 2013
dbSNP: rs4778889
rs4778889
IL16
0.683 0.480 15 81296654 intron variant T/C snv 0.24
CUI: C0014175
Disease: Endometriosis
Endometriosis 		0.010 1.000 1 2010 2010
dbSNP: rs4778889
rs4778889
IL16
0.683 0.480 15 81296654 intron variant T/C snv 0.24
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach 		0.010 1.000 1 2013 2013
dbSNP: rs4778889
rs4778889
IL16
0.683 0.480 15 81296654 intron variant T/C snv 0.24
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		0.010 1.000 1 2011 2011
dbSNP: rs4778889
rs4778889
IL16
0.683 0.480 15 81296654 intron variant T/C snv 0.24
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma 		0.010 1.000 1 2011 2011
dbSNP: rs4778889
rs4778889
IL16
0.683 0.480 15 81296654 intron variant T/C snv 0.24
CUI: C0029463
Disease: Osteosarcoma
Osteosarcoma 		0.010 < 0.001 1 2016 2016
dbSNP: rs4778889
rs4778889
IL16
0.683 0.480 15 81296654 intron variant T/C snv 0.24
CUI: C0585442
Disease: Osteosarcoma of bone
Osteosarcoma of bone 		0.010 < 0.001 1 2016 2016
dbSNP: rs4778889
rs4778889
IL16
0.683 0.480 15 81296654 intron variant T/C snv 0.24
CUI: C1332986
Disease: Childhood Osteosarcoma
Childhood Osteosarcoma 		0.010 < 0.001 1 2016 2016
dbSNP: rs4778889
rs4778889
IL16
0.683 0.480 15 81296654 intron variant T/C snv 0.24
CUI: C0030193
Disease: Pain
Pain 		0.010 1.000 1 2010 2010
dbSNP: rs4778889
rs4778889
IL16
0.683 0.480 15 81296654 intron variant T/C snv 0.24
CUI: C0011847
Disease: Diabetes
Diabetes 		0.010 1.000 1 2015 2015
dbSNP: rs4778889
rs4778889
IL16
0.683 0.480 15 81296654 intron variant T/C snv 0.24
CUI: C0011849
Disease: Diabetes Mellitus
Diabetes Mellitus 		0.010 1.000 1 2015 2015
dbSNP: rs4778889
rs4778889
IL16
0.683 0.480 15 81296654 intron variant T/C snv 0.24
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		0.010 1.000 1 2015 2015
dbSNP: rs4778889
rs4778889
IL16
0.683 0.480 15 81296654 intron variant T/C snv 0.24
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		0.010 1.000 1 2011 2011
dbSNP: rs4778889
rs4778889
IL16
0.683 0.480 15 81296654 intron variant T/C snv 0.24
CUI: C0409959
Disease: Osteoarthritis, Knee
Osteoarthritis, Knee 		0.010 1.000 1 2015 2015
dbSNP: rs4778889
rs4778889
IL16
0.683 0.480 15 81296654 intron variant T/C snv 0.24
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic 		0.010 1.000 1 2009 2009
dbSNP: rs4778889
rs4778889
IL16
0.683 0.480 15 81296654 intron variant T/C snv 0.24
CUI: C0018213
Disease: Graves Disease
Graves Disease 		0.010 1.000 1 2008 2008