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: rs113129609
rs113129609
IL1A
0.925 0.080 2 112778091 missense variant A/G snv
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		0.010 < 0.001 1 2003 2003
dbSNP: rs1516792
rs1516792
IL1A
0.925 0.080 2 112778356 intron variant G/A snv
CUI: C0022661
Disease: Kidney Failure, Chronic
Kidney Failure, Chronic 		0.010 1.000 1 2003 2003
dbSNP: rs1516792
rs1516792
IL1A
0.925 0.080 2 112778356 intron variant G/A snv
CUI: C2316810
Disease: Chronic kidney disease stage 5
Chronic kidney disease stage 5 		0.010 1.000 1 2003 2003
dbSNP: rs16347
rs16347
IL1A
0.925 0.080 2 112774138 3 prime UTR variant -/TGAA delins 0.70
CUI: C2316810
Disease: Chronic kidney disease stage 5
Chronic kidney disease stage 5 		0.010 1.000 1 2003 2003
dbSNP: rs16347
rs16347
IL1A
0.925 0.080 2 112774138 3 prime UTR variant -/TGAA delins 0.70
CUI: C0022661
Disease: Kidney Failure, Chronic
Kidney Failure, Chronic 		0.010 1.000 1 2003 2003
dbSNP: rs17561
rs17561
IL1A
0.672 0.560 2 112779646 missense variant C/A snv 0.27 0.26
CUI: C0242379
Disease: Malignant neoplasm of lung
Malignant neoplasm of lung 		0.010 1.000 1 2007 2007
dbSNP: rs17561
rs17561
IL1A
0.672 0.560 2 112779646 missense variant C/A snv 0.27 0.26
CUI: C0684249
Disease: Carcinoma of lung
Carcinoma of lung 		0.010 1.000 1 2007 2007
dbSNP: rs17561
rs17561
IL1A
0.672 0.560 2 112779646 missense variant C/A snv 0.27 0.26
CUI: C1306460
Disease: Primary malignant neoplasm of lung
Primary malignant neoplasm of lung 		0.010 1.000 1 2007 2007
dbSNP: rs17561
rs17561
IL1A
0.672 0.560 2 112779646 missense variant C/A snv 0.27 0.26
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma 		0.010 1.000 1 2007 2007
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: C0010068
Disease: Coronary heart disease
Coronary heart disease 		0.010 1.000 1 2008 2008
dbSNP: rs2071374
rs2071374
IL1A
1.000 0.120 2 112779775 intron variant T/G snv 0.27
CUI: C1384600
Disease: Systemic onset juvenile chronic arthritis
Systemic onset juvenile chronic arthritis 		0.010 1.000 1 2008 2008
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: rs17561
rs17561
IL1A
0.672 0.560 2 112779646 missense variant C/A snv 0.27 0.26
CUI: C0149931
Disease: Migraine Disorders
Migraine Disorders 		0.010 1.000 1 2010 2010
dbSNP: rs1800587
rs1800587
IL1A
0.620 0.720 2 112785383 upstream gene variant G/A;C snv 0.32
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.010 < 0.001 1 2010 2010
dbSNP: rs2071373
rs2071373
IL1A
1.000 2 112782507 intron variant G/A snv 0.74
CUI: C0741975
Disease: carotid disease
carotid disease 		0.010 1.000 1 2010 2010
dbSNP: rs2856836
rs2856836
IL1A
0.763 0.280 2 112774506 3 prime UTR variant A/G snv 0.26
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast 		0.010 1.000 1 2010 2010
dbSNP: rs2856836
rs2856836
IL1A
0.763 0.280 2 112774506 3 prime UTR variant A/G snv 0.26
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma 		0.010 1.000 1 2010 2010
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: C0025281
Disease: Meniere Disease
Meniere Disease 		0.010 1.000 1 2011 2011
dbSNP: rs3783553
rs3783553
IL1A
0.667 0.480 2 112774138 3 prime UTR variant -/TGAA delins
CUI: C2931822
Disease: Nasopharyngeal carcinoma
Nasopharyngeal carcinoma 		0.010 1.000 1 2011 2011
dbSNP: rs1894399
rs1894399
IL1A
0.925 0.040 2 112782600 intron variant C/T snv 0.32
CUI: C0038013
Disease: Ankylosing spondylitis
Ankylosing spondylitis 		0.020 1.000 2 2012 2012
dbSNP: rs17561
rs17561
IL1A
0.672 0.560 2 112779646 missense variant C/A snv 0.27 0.26
CUI: C0038013
Disease: Ankylosing spondylitis
Ankylosing spondylitis 		0.010 1.000 1 2012 2012
dbSNP: rs1800587
rs1800587
IL1A
0.620 0.720 2 112785383 upstream gene variant G/A;C snv 0.32
CUI: C0035851
Disease: Root Resorption
Root Resorption 		0.010 1.000 1 2012 2012
dbSNP: rs1894399
rs1894399
IL1A
0.925 0.040 2 112782600 intron variant C/T snv 0.32
CUI: C0949690
Disease: Spondylarthritis
Spondylarthritis 		0.010 1.000 1 2012 2012