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: rs2071375
rs2071375
IL1A
1.000 0.080 2 112777861 intron variant C/T snv 0.26
CUI: C0029456
Disease: Osteoporosis
Osteoporosis 		0.010 1.000 1 2012 2012
dbSNP: rs2856836
rs2856836
IL1A
0.763 0.280 2 112774506 3 prime UTR variant A/G snv 0.26
CUI: C0038013
Disease: Ankylosing spondylitis
Ankylosing spondylitis 		0.010 1.000 1 2012 2012
dbSNP: rs2856836
rs2856836
IL1A
0.763 0.280 2 112774506 3 prime UTR variant A/G snv 0.26
CUI: C0949690
Disease: Spondylarthritis
Spondylarthritis 		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: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease 		0.030 0.667 3 2009 2013
dbSNP: rs17561
rs17561
IL1A
0.672 0.560 2 112779646 missense variant C/A snv 0.27 0.26
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		0.020 1.000 2 2011 2013
dbSNP: rs1800587
rs1800587
IL1A
0.620 0.720 2 112785383 upstream gene variant G/A;C snv 0.32
CUI: C0011265
Disease: Presenile dementia
Presenile dementia 		0.020 1.000 2 2012 2013
dbSNP: rs1800587
rs1800587
IL1A
0.620 0.720 2 112785383 upstream gene variant G/A;C snv 0.32
CUI: C0497327
Disease: Dementia
Dementia 		0.020 1.000 2 2012 2013
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: 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: 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: 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: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		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: C0344315
Disease: Depressed mood
Depressed mood 		0.010 1.000 1 2013 2013
dbSNP: rs3783553
rs3783553
IL1A
0.667 0.480 2 112774138 3 prime UTR variant -/TGAA delins
CUI: C0014175
Disease: Endometriosis
Endometriosis 		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: C0019270
Disease: Hernia
Hernia 		0.020 1.000 2 2014 2014
dbSNP: rs3783553
rs3783553
IL1A
0.667 0.480 2 112774138 3 prime UTR variant -/TGAA delins
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma 		0.020 1.000 2 2009 2014
dbSNP: rs17561
rs17561
IL1A
0.672 0.560 2 112779646 missense variant C/A snv 0.27 0.26
CUI: C1140680
Disease: Malignant neoplasm of ovary
Malignant neoplasm of ovary 		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: C0302592
Disease: Cervix carcinoma
Cervix carcinoma 		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: C0919267
Disease: ovarian neoplasm
ovarian neoplasm 		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: C4721610
Disease: Carcinoma, Ovarian Epithelial
Carcinoma, Ovarian Epithelial 		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: 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: 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: C0011847
Disease: Diabetes
Diabetes 		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: C0011849
Disease: Diabetes Mellitus
Diabetes Mellitus 		0.010 1.000 1 2014 2014