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: rs1800795
rs1800795
0.494 0.840 7 22727026 intron variant C/G snv 0.71
CUI: C1302401
Disease: Adenoma of large intestine
Adenoma of large intestine
0.010 1.000 1 2010 2010
dbSNP: rs1800796
rs1800796
0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02
CUI: C0742343
Disease: Acute Chest Syndrome
Acute Chest Syndrome
0.010 1.000 1 2010 2010
dbSNP: rs1800796
rs1800796
0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02
CUI: C0948089
Disease: Acute Coronary Syndrome
Acute Coronary Syndrome
0.010 1.000 1 2010 2010
dbSNP: rs1800796
rs1800796
0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02
CUI: C0017665
Disease: Membranous glomerulonephritis
Membranous glomerulonephritis
0.010 1.000 1 2010 2010
dbSNP: rs1800797
rs1800797
0.605 0.800 7 22726602 non coding transcript exon variant A/G snv 0.72
CUI: C0007102
Disease: Malignant tumor of colon
Malignant tumor of colon
0.010 1.000 1 2010 2010
dbSNP: rs1800797
rs1800797
0.605 0.800 7 22726602 non coding transcript exon variant A/G snv 0.72
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X
0.010 1.000 1 2010 2010
dbSNP: rs1800797
rs1800797
0.605 0.800 7 22726602 non coding transcript exon variant A/G snv 0.72
CUI: C0020456
Disease: Hyperglycemia
Hyperglycemia
0.010 1.000 1 2010 2010
dbSNP: rs1800797
rs1800797
0.605 0.800 7 22726602 non coding transcript exon variant A/G snv 0.72
CUI: C0699790
Disease: Colon Carcinoma
Colon Carcinoma
0.010 1.000 1 2010 2010
dbSNP: rs13306435
rs13306435
IL6
1.000 0.080 7 22731420 missense variant T/A;C snv 2.9E-02; 4.2E-06
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.010 1.000 1 2011 2011
dbSNP: rs1800795
rs1800795
0.494 0.840 7 22727026 intron variant C/G snv 0.71
CUI: C0151744
Disease: Myocardial Ischemia
Myocardial Ischemia
0.010 1.000 1 2011 2011
dbSNP: rs1800796
rs1800796
0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02
CUI: C0151744
Disease: Myocardial Ischemia
Myocardial Ischemia
0.010 1.000 1 2011 2011
dbSNP: rs1800796
rs1800796
0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02
CUI: C0158266
Disease: Intervertebral Disc Degeneration
Intervertebral Disc Degeneration
0.010 1.000 1 2011 2011
dbSNP: rs1800797
rs1800797
0.605 0.800 7 22726602 non coding transcript exon variant A/G snv 0.72
CUI: C0011206
Disease: Delirium
Delirium
0.010 < 0.001 1 2011 2011
dbSNP: rs1800797
rs1800797
0.605 0.800 7 22726602 non coding transcript exon variant A/G snv 0.72
CUI: C0023343
Disease: Leprosy
Leprosy
0.010 1.000 1 2011 2011
dbSNP: rs2069825
rs2069825
1.000 0.040 7 22725718 non coding transcript exon variant -/CC delins 6.7E-05
CUI: C0024117
Disease: Chronic Obstructive Airway Disease
Chronic Obstructive Airway Disease
0.010 1.000 1 2011 2011
dbSNP: rs2069825
rs2069825
1.000 0.040 7 22725718 non coding transcript exon variant -/CC delins 6.7E-05
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases
0.010 1.000 1 2011 2011
dbSNP: rs2069861
rs2069861
IL6
0.925 0.080 7 22732035 upstream gene variant C/A;T snv
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
0.010 1.000 1 2011 2011
dbSNP: rs2069861
rs2069861
IL6
0.925 0.080 7 22732035 upstream gene variant C/A;T snv
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast
0.010 1.000 1 2011 2011
dbSNP: rs369953112
rs369953112
IL6
1.000 0.040 7 22731416 missense variant T/C snv
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X
0.010 1.000 1 2011 2011
dbSNP: rs1800795
rs1800795
0.494 0.840 7 22727026 intron variant C/G snv 0.71
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.020 1.000 2 2009 2012
dbSNP: rs1800795
rs1800795
0.494 0.840 7 22727026 intron variant C/G snv 0.71
CUI: C0015672
Disease: Fatigue
Fatigue
0.020 1.000 2 2011 2012
dbSNP: rs747126003
rs747126003
0.689 0.400 7 22728790 missense variant A/G;T snv 4.0E-06
CUI: C0028754
Disease: Obesity
Obesity
0.020 0.500 2 2009 2012
dbSNP: rs13306436
rs13306436
IL6
7 22731677 3 prime UTR variant G/A snv 7.2E-04
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement
0.700 1.000 1 2012 2012
dbSNP: rs13306436
rs13306436
IL6
7 22731677 3 prime UTR variant G/A snv 7.2E-04
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.700 1.000 1 2012 2012
dbSNP: rs13306436
rs13306436
IL6
7 22731677 3 prime UTR variant G/A snv 7.2E-04
High density lipoprotein measurement
0.700 1.000 1 2012 2012