IL1B, interleukin 1 beta, 3553

N. diseases: 1801; 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: rs1143627
rs1143627 		0.605 0.760 2 112836810 5 prime UTR variant G/A snv 0.56
CUI: C4016230
Disease: GASTRIC CANCER SUSCEPTIBILITY AFTER H. PYLORI INFECTION
GASTRIC CANCER SUSCEPTIBILITY AFTER H. PYLORI INFECTION 		0.700 0
dbSNP: rs1143627
rs1143627 		0.605 0.760 2 112836810 5 prime UTR variant G/A snv 0.56
CUI: C0026691
Disease: Mucocutaneous Lymph Node Syndrome
Mucocutaneous Lymph Node Syndrome 		Skin and Connective Tissue Diseases; Hemic and Lymphatic Diseases; Cardiovascular Diseases 0.010 < 0.001 1 2019 2019
dbSNP: rs1143627
rs1143627 		0.605 0.760 2 112836810 5 prime UTR variant G/A snv 0.56
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach 		Digestive System Diseases; Neoplasms 0.010 < 0.001 1 2018 2018
dbSNP: rs1143627
rs1143627 		0.605 0.760 2 112836810 5 prime UTR variant G/A snv 0.56
CUI: C0031090
Disease: Periodontal Diseases
Periodontal Diseases 		Stomatognathic Diseases 0.010 < 0.001 1 2017 2017
dbSNP: rs1143627
rs1143627 		0.605 0.760 2 112836810 5 prime UTR variant G/A snv 0.56
CUI: C0243026
Disease: Sepsis
Sepsis 		Pathological Conditions, Signs and Symptoms; Infections 0.010 < 0.001 1 2014 2014
dbSNP: rs1143627
rs1143627 		0.605 0.760 2 112836810 5 prime UTR variant G/A snv 0.56
CUI: C0036690
Disease: Septicemia
Septicemia 		Pathological Conditions, Signs and Symptoms; Infections 0.010 < 0.001 1 2014 2014
dbSNP: rs1143627
rs1143627 		0.605 0.760 2 112836810 5 prime UTR variant G/A snv 0.56
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma 		Digestive System Diseases; Neoplasms 0.010 < 0.001 1 2018 2018
dbSNP: rs1143634
rs1143634 		0.597 0.680 2 112832813 synonymous variant G/A snv 0.19 0.19
CUI: C0038013
Disease: Ankylosing spondylitis
Ankylosing spondylitis 		Musculoskeletal Diseases 0.010 < 0.001 1 2011 2011
dbSNP: rs1143634
rs1143634 		0.597 0.680 2 112832813 synonymous variant G/A snv 0.19 0.19
CUI: C0029410
Disease: Osteoarthritis of hip
Osteoarthritis of hip 		Musculoskeletal Diseases 0.010 < 0.001 1 2011 2011
dbSNP: rs16944
rs16944 		0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57
CUI: C0038013
Disease: Ankylosing spondylitis
Ankylosing spondylitis 		Musculoskeletal Diseases 0.010 < 0.001 1 2011 2011
dbSNP: rs16944
rs16944 		0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach 		Digestive System Diseases; Neoplasms 0.010 < 0.001 1 2018 2018
dbSNP: rs16944
rs16944 		0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder 		Mental Disorders 0.010 < 0.001 1 2010 2010
dbSNP: rs16944
rs16944 		0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57
CUI: C0021400
Disease: Influenza
Influenza 		Infections; Respiratory Tract Diseases 0.010 < 0.001 1 2019 2019
dbSNP: rs16944
rs16944 		0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57
CUI: C0026691
Disease: Mucocutaneous Lymph Node Syndrome
Mucocutaneous Lymph Node Syndrome 		Skin and Connective Tissue Diseases; Hemic and Lymphatic Diseases; Cardiovascular Diseases 0.010 < 0.001 1 2019 2019
dbSNP: rs16944
rs16944 		0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma 		Digestive System Diseases; Neoplasms 0.010 < 0.001 1 2018 2018
dbSNP: rs16944
rs16944 		0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57
CUI: C0029410
Disease: Osteoarthritis of hip
Osteoarthritis of hip 		Musculoskeletal Diseases 0.010 < 0.001 1 2011 2011
dbSNP: rs16944
rs16944 		0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57
CUI: C0014544
Disease: Epilepsy
Epilepsy 		Nervous System Diseases 0.010 < 0.001 1 2012 2012
dbSNP: rs16944
rs16944 		0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57
CUI: C0001339
Disease: Acute pancreatitis
Acute pancreatitis 		Digestive System Diseases 0.010 < 0.001 1 2013 2013
dbSNP: rs3917356
rs3917356 		0.882 0.160 2 112834786 intron variant C/T snv 0.39
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma 		Digestive System Diseases; Neoplasms 0.010 < 0.001 1 2018 2018
dbSNP: rs1143634
rs1143634 		0.597 0.680 2 112832813 synonymous variant G/A snv 0.19 0.19
CUI: C0031090
Disease: Periodontal Diseases
Periodontal Diseases 		Stomatognathic Diseases 0.030 0.333 3 2014 2019
dbSNP: rs1143634
rs1143634 		0.597 0.680 2 112832813 synonymous variant G/A snv 0.19 0.19
CUI: C0001339
Disease: Acute pancreatitis
Acute pancreatitis 		Digestive System Diseases 0.020 0.500 2 2013 2015
dbSNP: rs16944
rs16944 		0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57
CUI: C0036690
Disease: Septicemia
Septicemia 		Pathological Conditions, Signs and Symptoms; Infections 0.020 0.500 2 2014 2016
dbSNP: rs16944
rs16944 		0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57
CUI: C0243026
Disease: Sepsis
Sepsis 		Pathological Conditions, Signs and Symptoms; Infections 0.020 0.500 2 2014 2016
dbSNP: rs16944
rs16944 		0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57
CUI: C0015672
Disease: Fatigue
Fatigue 		Pathological Conditions, Signs and Symptoms 0.020 0.500 2 2011 2012
dbSNP: rs16944
rs16944 		0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57
CUI: C0031090
Disease: Periodontal Diseases
Periodontal Diseases 		Stomatognathic Diseases 0.020 0.500 2 2014 2019