IL6, interleukin 6, 3569

N. diseases: 2367; N. variants: 22
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class 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: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		Nutritional and Metabolic Diseases; Endocrine System Diseases 0.070 1.000 7 2006 2018
dbSNP: rs1800795
rs1800795 		0.494 0.840 7 22727026 intron variant C/G snv 0.71
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma 		Neoplasms; Skin and Connective Tissue Diseases 0.060 1.000 6 2007 2017
dbSNP: rs1800795
rs1800795 		0.494 0.840 7 22727026 intron variant C/G snv 0.71
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast 		Neoplasms; Skin and Connective Tissue Diseases 0.060 1.000 6 2007 2017
dbSNP: rs1800795
rs1800795 		0.494 0.840 7 22727026 intron variant C/G snv 0.71
CUI: C0027651
Disease: Neoplasms
Neoplasms 		Neoplasms 0.050 1.000 5 2009 2017
dbSNP: rs1800795
rs1800795 		0.494 0.840 7 22727026 intron variant C/G snv 0.71
CUI: C0041296
Disease: Tuberculosis
Tuberculosis 		Infections 0.040 1.000 4 2018 2020
dbSNP: rs1800795
rs1800795 		0.494 0.840 7 22727026 intron variant C/G snv 0.71
CUI: C0007847
Disease: Malignant tumor of cervix
Malignant tumor of cervix 		Neoplasms; Female Urogenital Diseases and Pregnancy Complications 0.040 1.000 4 2017 2018
dbSNP: rs1800795
rs1800795 		0.494 0.840 7 22727026 intron variant C/G snv 0.71
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		Cardiovascular Diseases 0.040 1.000 4 2014 2019
dbSNP: rs1800795
rs1800795 		0.494 0.840 7 22727026 intron variant C/G snv 0.71
CUI: C0302592
Disease: Cervix carcinoma
Cervix carcinoma 		Neoplasms; Female Urogenital Diseases and Pregnancy Complications 0.040 1.000 4 2017 2018
dbSNP: rs1800795
rs1800795 		0.494 0.840 7 22727026 intron variant C/G snv 0.71
CUI: C4048328
Disease: cervical cancer
cervical cancer 		Neoplasms; Female Urogenital Diseases and Pregnancy Complications 0.040 1.000 4 2017 2018
dbSNP: rs1800796
rs1800796 		0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02
CUI: C0948008
Disease: Ischemic stroke
Ischemic stroke 		Nervous System Diseases; Cardiovascular Diseases 0.040 1.000 4 2011 2017
dbSNP: rs1800796
rs1800796 		0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach 		Digestive System Diseases; Neoplasms 0.040 1.000 4 2012 2019
dbSNP: rs1800796
rs1800796 		0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma 		Digestive System Diseases; Neoplasms 0.040 1.000 4 2012 2019
dbSNP: rs1800796
rs1800796 		0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		Nutritional and Metabolic Diseases; Endocrine System Diseases 0.040 1.000 4 2006 2017
dbSNP: rs1800796
rs1800796 		0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02
CUI: C0029456
Disease: Osteoporosis
Osteoporosis 		Nutritional and Metabolic Diseases; Musculoskeletal Diseases 0.040 1.000 4 2010 2019
dbSNP: rs1800795
rs1800795 		0.494 0.840 7 22727026 intron variant C/G snv 0.71
CUI: C0700095
Disease: Central neuroblastoma
Central neuroblastoma 		Neoplasms; Nervous System Diseases 0.030 1.000 3 2009 2018
dbSNP: rs1800795
rs1800795 		0.494 0.840 7 22727026 intron variant C/G snv 0.71
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		Digestive System Diseases; Neoplasms 0.030 1.000 3 2007 2016
dbSNP: rs1800795
rs1800795 		0.494 0.840 7 22727026 intron variant C/G snv 0.71
CUI: C0086132
Disease: Depressive Symptoms
Depressive Symptoms 		Behavior and Behavior Mechanisms 0.030 1.000 3 2010 2016
dbSNP: rs1800795
rs1800795 		0.494 0.840 7 22727026 intron variant C/G snv 0.71
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease 		Nervous System Diseases; Mental Disorders 0.720 1.000 3 2012 2016
dbSNP: rs1800795
rs1800795 		0.494 0.840 7 22727026 intron variant C/G snv 0.71
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		Mental Disorders 0.030 1.000 3 2012 2018
dbSNP: rs1800795
rs1800795 		0.494 0.840 7 22727026 intron variant C/G snv 0.71
CUI: C0029408
Disease: Degenerative polyarthritis
Degenerative polyarthritis 		Musculoskeletal Diseases 0.030 1.000 3 2008 2014
dbSNP: rs1800795
rs1800795 		0.494 0.840 7 22727026 intron variant C/G snv 0.71
CUI: C0027819
Disease: Neuroblastoma
Neuroblastoma 		Neoplasms 0.030 1.000 3 2009 2018
dbSNP: rs1800795
rs1800795 		0.494 0.840 7 22727026 intron variant C/G snv 0.71
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		Immune System Diseases; Nervous System Diseases 0.030 1.000 3 2011 2018
dbSNP: rs1800795
rs1800795 		0.494 0.840 7 22727026 intron variant C/G snv 0.71
CUI: C4086165
Disease: Childhood Neuroblastoma
Childhood Neuroblastoma 		Neoplasms 0.030 1.000 3 2009 2018
dbSNP: rs1800796
rs1800796 		0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms 		Neoplasms 0.030 1.000 3 2007 2018
dbSNP: rs1800796
rs1800796 		0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm 		Neoplasms 0.030 1.000 3 2007 2018