Source: ALL

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: rs17561
rs17561
IL1A
0.672 0.560 2 112779646 missense variant C/A snv 0.27 0.26
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.010 1.000 1 2016 2016
dbSNP: rs17561
rs17561
IL1A
0.672 0.560 2 112779646 missense variant C/A snv 0.27 0.26
CUI: C0221775
Disease: Lumbar disc disease
Lumbar disc disease 		0.010 1.000 1 2017 2017
dbSNP: rs17561
rs17561
IL1A
0.672 0.560 2 112779646 missense variant C/A snv 0.27 0.26
CUI: C4721610
Disease: Carcinoma, Ovarian Epithelial
Carcinoma, Ovarian Epithelial 		0.010 1.000 1 2014 2014
dbSNP: rs17561
rs17561
IL1A
0.672 0.560 2 112779646 missense variant C/A snv 0.27 0.26
CUI: C0024530
Disease: Malaria
Malaria 		0.010 1.000 1 2015 2015
dbSNP: rs17561
rs17561
IL1A
0.672 0.560 2 112779646 missense variant C/A snv 0.27 0.26
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast 		0.010 1.000 1 2007 2007
dbSNP: rs1800587
rs1800587
IL1A
0.620 0.720 2 112785383 upstream gene variant G/A;C snv 0.32
CUI: C0391826
Disease: Lhermitte-Duclos disease
Lhermitte-Duclos disease 		0.010 1.000 1 2017 2017
dbSNP: rs1800587
rs1800587
IL1A
0.620 0.720 2 112785383 upstream gene variant G/A;C snv 0.32
CUI: C0002895
Disease: Anemia, Sickle Cell
Anemia, Sickle Cell 		0.010 1.000 1 2016 2016
dbSNP: rs1800587
rs1800587
IL1A
0.620 0.720 2 112785383 upstream gene variant G/A;C snv 0.32
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms 		0.010 1.000 1 2019 2019
dbSNP: rs1800587
rs1800587
IL1A
0.620 0.720 2 112785383 upstream gene variant G/A;C snv 0.32
CUI: C0011570
Disease: Mental Depression
Mental Depression 		0.010 1.000 1 2013 2013
dbSNP: rs1800587
rs1800587
IL1A
0.620 0.720 2 112785383 upstream gene variant G/A;C snv 0.32
CUI: C0007847
Disease: Malignant tumor of cervix
Malignant tumor of cervix 		0.010 1.000 1 2019 2019
dbSNP: rs1800587
rs1800587
IL1A
0.620 0.720 2 112785383 upstream gene variant G/A;C snv 0.32
CUI: C4048328
Disease: cervical cancer
cervical cancer 		0.010 1.000 1 2019 2019
dbSNP: rs1800587
rs1800587
IL1A
0.620 0.720 2 112785383 upstream gene variant G/A;C snv 0.32
CUI: C0011854
Disease: Diabetes Mellitus, Insulin-Dependent
Diabetes Mellitus, Insulin-Dependent 		0.010 1.000 1 2016 2016
dbSNP: rs1800587
rs1800587
IL1A
0.620 0.720 2 112785383 upstream gene variant G/A;C snv 0.32
CUI: C4275242
Disease: Sudden sensorineural hearing loss
Sudden sensorineural hearing loss 		0.010 1.000 1 2011 2011
dbSNP: rs1800587
rs1800587
IL1A
0.620 0.720 2 112785383 upstream gene variant G/A;C snv 0.32
CUI: C0041696
Disease: Unipolar Depression
Unipolar Depression 		0.010 1.000 1 2013 2013
dbSNP: rs1800587
rs1800587
IL1A
0.620 0.720 2 112785383 upstream gene variant G/A;C snv 0.32
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X 		0.010 1.000 1 2009 2009
dbSNP: rs1800587
rs1800587
IL1A
0.620 0.720 2 112785383 upstream gene variant G/A;C snv 0.32
CUI: C0011581
Disease: Depressive disorder
Depressive disorder 		0.010 1.000 1 2013 2013
dbSNP: rs1800587
rs1800587
IL1A
0.620 0.720 2 112785383 upstream gene variant G/A;C snv 0.32
CUI: C0278147
Disease: Radicular pain
Radicular pain 		0.010 1.000 1 2014 2014
dbSNP: rs1800587
rs1800587
IL1A
0.620 0.720 2 112785383 upstream gene variant G/A;C snv 0.32
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder 		0.010 1.000 1 2013 2013
dbSNP: rs1800587
rs1800587
IL1A
0.620 0.720 2 112785383 upstream gene variant G/A;C snv 0.32
CUI: C0029408
Disease: Degenerative polyarthritis
Degenerative polyarthritis 		0.010 1.000 1 2013 2013
dbSNP: rs1800587
rs1800587
IL1A
0.620 0.720 2 112785383 upstream gene variant G/A;C snv 0.32
CUI: C3495798
Disease: Periodontal inflammation
Periodontal inflammation 		0.010 1.000 1 2019 2019
dbSNP: rs1800587
rs1800587
IL1A
0.620 0.720 2 112785383 upstream gene variant G/A;C snv 0.32
CUI: C0004364
Disease: Autoimmune Diseases
Autoimmune Diseases 		0.010 < 0.001 1 2018 2018
dbSNP: rs1800587
rs1800587
IL1A
0.620 0.720 2 112785383 upstream gene variant G/A;C snv 0.32
CUI: C0031090
Disease: Periodontal Diseases
Periodontal Diseases 		0.010 1.000 1 2014 2014
dbSNP: rs1800587
rs1800587
IL1A
0.620 0.720 2 112785383 upstream gene variant G/A;C snv 0.32
CUI: C0238694
Disease: Peripheral arthritis
Peripheral arthritis 		0.010 1.000 1 2019 2019
dbSNP: rs1800587
rs1800587
IL1A
0.620 0.720 2 112785383 upstream gene variant G/A;C snv 0.32
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm 		0.010 1.000 1 2019 2019
dbSNP: rs1800587
rs1800587
IL1A
0.620 0.720 2 112785383 upstream gene variant G/A;C snv 0.32
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		0.010 1.000 1 2008 2008