IL18R1, interleukin 18 receptor 1, 8809

N. diseases: 23; N. variants: 34
Source: GWASCAT ×
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: rs13015714
rs13015714 		0.882 0.200 2 102355405 intron variant G/T snv 0.77
CUI: C0007570
Disease: Celiac Disease
Celiac Disease 		Digestive System Diseases; Nutritional and Metabolic Diseases 0.810 1.000 1 2008 2009
dbSNP: rs1420101
rs1420101 		0.827 0.280 2 102341256 synonymous variant C/T snv 0.33 0.35
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure 		0.800 1.000 1 2009 2009
dbSNP: rs13408661
rs13408661 		1.000 0.080 2 102338622 intron variant G/A snv 0.18
CUI: C0004096
Disease: Asthma
Asthma 		Respiratory Tract Diseases; Immune System Diseases 0.810 1.000 1 2011 2012
dbSNP: rs3771166
rs3771166 		1.000 0.080 2 102369762 intron variant G/A;T snv
CUI: C0004096
Disease: Asthma
Asthma 		Respiratory Tract Diseases; Immune System Diseases 0.810 1.000 1 2010 2012
dbSNP: rs9807989
rs9807989 		1.000 0.080 2 102354740 intron variant T/C;G snv 0.46
CUI: C0004096
Disease: Asthma
Asthma 		Respiratory Tract Diseases; Immune System Diseases 0.800 1.000 1 2012 2012
dbSNP: rs10197862
rs10197862 		0.925 0.120 2 102350089 intron variant A/G snv 0.18
CUI: C0004096
Disease: Asthma
Asthma 		Respiratory Tract Diseases; Immune System Diseases 0.810 1.000 1 2011 2014
dbSNP: rs10197862
rs10197862 		0.925 0.120 2 102350089 intron variant A/G snv 0.18
CUI: C0018621
Disease: Hay fever
Hay fever 		Respiratory Tract Diseases; Immune System Diseases; Otorhinolaryngologic Diseases 0.700 1.000 1 2014 2014
dbSNP: rs13015714
rs13015714 		0.882 0.200 2 102355405 intron variant G/T snv 0.77
CUI: C0011615
Disease: Dermatitis, Atopic
Dermatitis, Atopic 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Immune System Diseases 0.800 1.000 2 2012 2015
dbSNP: rs1420098
rs1420098 		2 102367819 splice region variant T/C snv 0.35 0.33
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases 		Digestive System Diseases 0.700 1.000 1 2015 2015
dbSNP: rs76886731
rs76886731 		1.000 0.040 2 102328956 intron variant A/T snv 0.48
CUI: C0023343
Disease: Leprosy
Leprosy 		Infections 0.700 1.000 1 2015 2015
dbSNP: rs12987977
rs12987977 		0.827 0.120 2 102358876 intron variant T/G snv 0.31
CUI: C0033860
Disease: Psoriasis
Psoriasis 		Skin and Connective Tissue Diseases 0.700 1.000 1 2016 2016
dbSNP: rs12987977
rs12987977 		0.827 0.120 2 102358876 intron variant T/G snv 0.31
CUI: C0008313
Disease: Cholangitis, Sclerosing
Cholangitis, Sclerosing 		Digestive System Diseases 0.700 1.000 1 2016 2016
dbSNP: rs12987977
rs12987977 		0.827 0.120 2 102358876 intron variant T/G snv 0.31
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis 		Digestive System Diseases 0.700 1.000 1 2016 2016
dbSNP: rs12987977
rs12987977 		0.827 0.120 2 102358876 intron variant T/G snv 0.31
CUI: C0038013
Disease: Ankylosing spondylitis
Ankylosing spondylitis 		Musculoskeletal Diseases 0.700 1.000 1 2016 2016
dbSNP: rs12987977
rs12987977 		0.827 0.120 2 102358876 intron variant T/G snv 0.31
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		Digestive System Diseases 0.700 1.000 1 2016 2016
dbSNP: rs5833013
rs5833013 		2 102352407 intron variant -/TA delins
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure 		0.700 1.000 1 2016 2016
dbSNP: rs5833013
rs5833013 		2 102352407 intron variant -/TA delins
CUI: C0200641
Disease: Blood basophil count (lab test)
Blood basophil count (lab test) 		0.700 1.000 1 2016 2016
dbSNP: rs950881
rs950881 		1.000 0.120 2 102316052 intron variant G/A;T snv
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction 		Immune System Diseases 0.800 1.000 1 2013 2016
dbSNP: rs10865050
rs10865050 		2 102324851 intron variant G/A snv 0.18
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction 		Immune System Diseases 0.700 1.000 1 2017 2017
dbSNP: rs12712135
rs12712135 		2 102314488 intron variant A/G snv 0.55
CUI: C4553157
Disease: Interleukin 1 Receptor-Like 1 Measurement
Interleukin 1 Receptor-Like 1 Measurement 		0.700 1.000 1 2017 2017
dbSNP: rs13001325
rs13001325 		1.000 0.040 2 102322576 intron variant C/T snv 0.30
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases 		Digestive System Diseases 0.700 1.000 1 2017 2017
dbSNP: rs13001325
rs13001325 		1.000 0.040 2 102322576 intron variant C/T snv 0.30
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		Digestive System Diseases 0.700 1.000 1 2017 2017
dbSNP: rs3771167
rs3771167 		2 102369728 intron variant A/G snv 0.11
CUI: C4553157
Disease: Interleukin 1 Receptor-Like 1 Measurement
Interleukin 1 Receptor-Like 1 Measurement 		0.700 1.000 1 2017 2017
dbSNP: rs11676124
rs11676124 		2 102324878 intron variant T/C snv 0.66
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs13014644
rs13014644 		2 102354903 intron variant G/T snv 9.6E-02
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2018 2018