IL1RN, interleukin 1 receptor antagonist, 3557

N. diseases: 701; N. variants: 52
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: rs928940
rs928940 		0.882 0.120 2 113119918 intron variant G/T snv 0.78
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma 		Neoplasms; Skin and Connective Tissue Diseases 0.010 1.000 1 2017 2017
dbSNP: rs1457547311
rs1457547311 		0.851 0.080 2 113131082 synonymous variant G/A snv 4.0E-06
CUI: C0085695
Disease: Chronic gastritis
Chronic gastritis 		Digestive System Diseases 0.010 < 0.001 1 2012 2012
dbSNP: rs1457547311
rs1457547311 		0.851 0.080 2 113131082 synonymous variant G/A snv 4.0E-06
CUI: C0679408
Disease: Lesion of stomach
Lesion of stomach 		Digestive System Diseases 0.010 < 0.001 1 2013 2013
dbSNP: rs1457547311
rs1457547311 		0.851 0.080 2 113131082 synonymous variant G/A snv 4.0E-06
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma 		Digestive System Diseases; Neoplasms 0.010 < 0.001 1 2012 2012
dbSNP: rs1457547311
rs1457547311 		0.851 0.080 2 113131082 synonymous variant G/A snv 4.0E-06
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach 		Digestive System Diseases; Neoplasms 0.010 < 0.001 1 2012 2012
dbSNP: rs315919
rs315919 		0.851 0.120 2 113118636 intron variant T/G snv 0.55
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast 		Neoplasms; Skin and Connective Tissue Diseases 0.010 1.000 1 2017 2017
dbSNP: rs315919
rs315919 		0.851 0.120 2 113118636 intron variant T/G snv 0.55
CUI: C0152018
Disease: Esophageal carcinoma
Esophageal carcinoma 		Digestive System Diseases; Neoplasms 0.010 1.000 1 2019 2019
dbSNP: rs315919
rs315919 		0.851 0.120 2 113118636 intron variant T/G snv 0.55
CUI: C0546837
Disease: Malignant neoplasm of esophagus
Malignant neoplasm of esophagus 		Digestive System Diseases; Neoplasms 0.010 1.000 1 2019 2019
dbSNP: rs315919
rs315919 		0.851 0.120 2 113118636 intron variant T/G snv 0.55
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma 		Neoplasms; Skin and Connective Tissue Diseases 0.010 1.000 1 2017 2017
dbSNP: rs315919
rs315919 		0.851 0.120 2 113118636 intron variant T/G snv 0.55
CUI: C0014859
Disease: Esophageal Neoplasms
Esophageal Neoplasms 		Digestive System Diseases; Neoplasms 0.010 1.000 1 2019 2019
dbSNP: rs3181052
rs3181052 		0.851 0.120 2 113128472 intron variant G/A snv 0.16
CUI: C0152018
Disease: Esophageal carcinoma
Esophageal carcinoma 		Digestive System Diseases; Neoplasms 0.010 1.000 1 2019 2019
dbSNP: rs3181052
rs3181052 		0.851 0.120 2 113128472 intron variant G/A snv 0.16
CUI: C0546837
Disease: Malignant neoplasm of esophagus
Malignant neoplasm of esophagus 		Digestive System Diseases; Neoplasms 0.010 1.000 1 2019 2019
dbSNP: rs3181052
rs3181052 		0.851 0.120 2 113128472 intron variant G/A snv 0.16
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma 		Neoplasms; Skin and Connective Tissue Diseases 0.010 1.000 1 2017 2017
dbSNP: rs3181052
rs3181052 		0.851 0.120 2 113128472 intron variant G/A snv 0.16
CUI: C0014859
Disease: Esophageal Neoplasms
Esophageal Neoplasms 		Digestive System Diseases; Neoplasms 0.010 1.000 1 2019 2019
dbSNP: rs3181052
rs3181052 		0.851 0.120 2 113128472 intron variant G/A snv 0.16
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast 		Neoplasms; Skin and Connective Tissue Diseases 0.010 1.000 1 2017 2017
dbSNP: rs447713
rs447713 		0.851 0.160 2 113130095 non coding transcript exon variant A/G snv 0.21
CUI: C0004096
Disease: Asthma
Asthma 		Respiratory Tract Diseases; Immune System Diseases 0.010 1.000 1 2006 2006
dbSNP: rs447713
rs447713 		0.851 0.160 2 113130095 non coding transcript exon variant A/G snv 0.21
CUI: C3662483
Disease: Allergic sensitization
Allergic sensitization 		0.010 1.000 1 2006 2006
dbSNP: rs447713
rs447713 		0.851 0.160 2 113130095 non coding transcript exon variant A/G snv 0.21
CUI: C3815172
Disease: Interleukin 1 Beta Measurement
Interleukin 1 Beta Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs447713
rs447713 		0.851 0.160 2 113130095 non coding transcript exon variant A/G snv 0.21
CUI: C0035439
Disease: Rheumatic Heart Disease
Rheumatic Heart Disease 		Infections; Cardiovascular Diseases 0.010 1.000 1 2016 2016
dbSNP: rs447713
rs447713 		0.851 0.160 2 113130095 non coding transcript exon variant A/G snv 0.21
CUI: C0869523
Disease: Carditis
Carditis 		Cardiovascular Diseases 0.010 1.000 1 2016 2016
dbSNP: rs9005
rs9005 		0.851 0.160 2 113133835 3 prime UTR variant G/A snv 0.29
CUI: C0029410
Disease: Osteoarthritis of hip
Osteoarthritis of hip 		Musculoskeletal Diseases 0.010 1.000 1 2011 2011
dbSNP: rs9005
rs9005 		0.851 0.160 2 113133835 3 prime UTR variant G/A snv 0.29
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		Mental Disorders 0.010 1.000 1 2016 2016
dbSNP: rs9005
rs9005 		0.851 0.160 2 113133835 3 prime UTR variant G/A snv 0.29
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach 		Digestive System Diseases; Neoplasms 0.010 1.000 1 2015 2015
dbSNP: rs9005
rs9005 		0.851 0.160 2 113133835 3 prime UTR variant G/A snv 0.29
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma 		Digestive System Diseases; Neoplasms 0.010 1.000 1 2015 2015
dbSNP: rs452204
rs452204 		0.807 0.200 2 113131484 intron variant G/A snv 0.45
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma 		Neoplasms; Skin and Connective Tissue Diseases 0.010 1.000 1 2017 2017