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: rs13306435
rs13306435
IL6
1.000 0.071 7 22731420 missense variant T/A,C snp 2.9E-02; 4.2E-06 1.5E-02
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.010 1.000 1 2011 2011
dbSNP: rs1474347
rs1474347
1.000 0.107 7 22728505 non coding transcript exon variant C/A snp 0.66
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
0.010 1.000 1 2015 2015
dbSNP: rs1524107
rs1524107
0.923 0.214 7 22728600 non coding transcript exon variant C/T snp 9.8E-02
Diabetes Mellitus, Non-Insulin-Dependent
0.010 1.000 1 2016 2016
dbSNP: rs1524107
rs1524107
0.923 0.214 7 22728600 non coding transcript exon variant C/T snp 9.8E-02
CUI: C0022658
Disease: Kidney Diseases
Kidney Diseases
0.010 1.000 1 2016 2016
dbSNP: rs1524107
rs1524107
0.923 0.214 7 22728600 non coding transcript exon variant C/T snp 9.8E-02
CUI: C1857276
Disease: Trichohepatoenteric Syndrome
Trichohepatoenteric Syndrome
0.010 1.000 1 2011 2011
dbSNP: rs1800795
rs1800795
0.580 0.607 7 22727026 intron variant C/G snp 0.68
CUI: C0011849
Disease: Diabetes Mellitus
Diabetes Mellitus
0.010 1.000 1 2006 2006
dbSNP: rs1800795
rs1800795
0.580 0.607 7 22727026 intron variant C/G snp 0.68
CUI: C0338656
Disease: Impaired cognition
Impaired cognition
0.010 1.000 1 2017 2017
dbSNP: rs1800795
rs1800795
0.580 0.607 7 22727026 intron variant C/G snp 0.68
CUI: C0856825
Disease: Acute GVH disease
Acute GVH disease
0.010 1.000 1 2012 2012
dbSNP: rs1800795
rs1800795
0.580 0.607 7 22727026 intron variant C/G snp 0.68
CUI: C0022658
Disease: Kidney Diseases
Kidney Diseases
0.010 1.000 1 2009 2009
dbSNP: rs1800795
rs1800795
0.580 0.607 7 22727026 intron variant C/G snp 0.68
CUI: C0003850
Disease: Arteriosclerosis
Arteriosclerosis
0.010 1.000 1 2014 2014
dbSNP: rs1800795
rs1800795
0.580 0.607 7 22727026 intron variant C/G snp 0.68
CUI: C0007847
Disease: Malignant tumor of cervix
Malignant tumor of cervix
0.010 1.000 1 2018 2018
dbSNP: rs1800795
rs1800795
0.580 0.607 7 22727026 intron variant C/G snp 0.68
CUI: C0948008
Disease: Ischemic stroke
Ischemic stroke
0.010 1.000 1 2016 2016
dbSNP: rs1800795
rs1800795
0.580 0.607 7 22727026 intron variant C/G snp 0.68
CUI: C0242339
Disease: Dyslipidemias
Dyslipidemias
0.010 1.000 1 2016 2016
dbSNP: rs1800795
rs1800795
0.580 0.607 7 22727026 intron variant C/G snp 0.68
Chronic Lymphocytic Leukemia/Small Lymphocytic Lymphoma
0.010 1.000 1 2016 2016
dbSNP: rs1800795
rs1800795
0.580 0.607 7 22727026 intron variant C/G snp 0.68
CUI: C0007789
Disease: Cerebral Palsy
Cerebral Palsy
0.010 1.000 1 2011 2011
dbSNP: rs1800795
rs1800795
0.580 0.607 7 22727026 intron variant C/G snp 0.68
CUI: C4048328
Disease: cervical cancer
cervical cancer
0.010 1.000 1 2018 2018
dbSNP: rs1800795
rs1800795
0.580 0.607 7 22727026 intron variant C/G snp 0.68
CUI: C0036421
Disease: Systemic Scleroderma
Systemic Scleroderma
0.010 1.000 1 2013 2013
dbSNP: rs1800795
rs1800795
0.580 0.607 7 22727026 intron variant C/G snp 0.68
CUI: C0011881
Disease: Diabetic Nephropathy
Diabetic Nephropathy
0.010 1.000 1 2016 2016
dbSNP: rs1800795
rs1800795
0.580 0.607 7 22727026 intron variant C/G snp 0.68
Necrotizing enterocolitis in fetus OR newborn
0.010 1.000 1 2016 2016
dbSNP: rs1800795
rs1800795
0.580 0.607 7 22727026 intron variant C/G snp 0.68
CUI: C0011269
Disease: Dementia, Vascular
Dementia, Vascular
0.010 1.000 1 2012 2012
dbSNP: rs1800795
rs1800795
0.580 0.607 7 22727026 intron variant C/G snp 0.68
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
0.010 1.000 1 2018 2018
dbSNP: rs1800795
rs1800795
0.580 0.607 7 22727026 intron variant C/G snp 0.68
CUI: C0004153
Disease: Atherosclerosis
Atherosclerosis
0.010 1.000 1 2014 2014
dbSNP: rs1800795
rs1800795
0.580 0.607 7 22727026 intron variant C/G snp 0.68
Systemic Inflammatory Response Syndrome
0.010 1.000 1 2015 2015
dbSNP: rs1800795
rs1800795
0.580 0.607 7 22727026 intron variant C/G snp 0.68
CUI: C0004610
Disease: Bacteremia
Bacteremia
0.010 1.000 1 2016 2016
dbSNP: rs1800795
rs1800795
0.580 0.607 7 22727026 intron variant C/G snp 0.68
CUI: C0302592
Disease: Cervix carcinoma
Cervix carcinoma
0.010 1.000 1 2018 2018