IL1RL1, interleukin 1 receptor like 1, 9173

N. diseases: 117; N. variants: 51
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: rs17639215
rs17639215 		2 102336984 intron variant G/A snv 9.7E-02
CUI: C0043144
Disease: Wheezing
Wheezing 		Pathological Conditions, Signs and Symptoms 0.010 1.000 1 2014 2014
dbSNP: rs6543115
rs6543115 		1.000 0.040 2 102311181 upstream gene variant C/A;G snv
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis 		Digestive System Diseases 0.010 1.000 1 2017 2017
dbSNP: rs6543116
rs6543116 		0.882 0.120 2 102311266 upstream gene variant A/G snv 0.76
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis 		Digestive System Diseases 0.010 1.000 1 2017 2017
dbSNP: rs59185885
rs59185885 		1.000 0.040 2 102327786 intron variant T/G snv 0.18
CUI: C0035242
Disease: Respiratory Tract Diseases
Respiratory Tract Diseases 		Respiratory Tract Diseases 0.700 1.000 1 2019 2019
dbSNP: rs950880
rs950880 		1.000 0.040 2 102316102 intron variant C/A snv 0.30
CUI: C1704436
Disease: Peripheral Arterial Diseases
Peripheral Arterial Diseases 		Cardiovascular Diseases 0.010 1.000 1 2017 2017
dbSNP: rs3821204
rs3821204 		0.807 0.160 2 102343821 3 prime UTR variant C/G snv 0.21
CUI: C0585442
Disease: Osteosarcoma of bone
Osteosarcoma of bone 		Neoplasms 0.010 1.000 1 2018 2018
dbSNP: rs3821204
rs3821204 		0.807 0.160 2 102343821 3 prime UTR variant C/G snv 0.21
CUI: C0029463
Disease: Osteosarcoma
Osteosarcoma 		Neoplasms 0.010 1.000 1 2018 2018
dbSNP: rs1420101
rs1420101 		0.827 0.280 2 102341256 synonymous variant C/T snv 0.33 0.35
CUI: C0027430
Disease: Nasal Polyps
Nasal Polyps 		Pathological Conditions, Signs and Symptoms; Respiratory Tract Diseases; Otorhinolaryngologic Diseases 0.710 0.500 2 2010 2019
dbSNP: rs3821204
rs3821204 		0.807 0.160 2 102343821 3 prime UTR variant C/G snv 0.21
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma 		Digestive System Diseases; Neoplasms 0.010 1.000 1 2019 2019
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: rs12470864
rs12470864 		0.925 0.080 2 102309902 upstream gene variant G/A snv 0.30
CUI: C4553157
Disease: Interleukin 1 Receptor-Like 1 Measurement
Interleukin 1 Receptor-Like 1 Measurement 		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: rs3821204
rs3821204 		0.807 0.160 2 102343821 3 prime UTR variant C/G snv 0.21
CUI: C1512409
Disease: Hepatocarcinogenesis
Hepatocarcinogenesis 		Pathological Conditions, Signs and Symptoms; Neoplasms 0.010 1.000 1 2019 2019
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: rs6543116
rs6543116 		0.882 0.120 2 102311266 upstream gene variant A/G snv 0.76
CUI: C0677607
Disease: Hashimoto Disease
Hashimoto Disease 		Endocrine System Diseases 0.010 1.000 1 2016 2016
dbSNP: rs11685424
rs11685424 		0.925 0.040 2 102310521 upstream gene variant G/A snv 0.54
CUI: C0085580
Disease: Essential Hypertension
Essential Hypertension 		Cardiovascular Diseases 0.010 1.000 1 2017 2017
dbSNP: rs3821204
rs3821204 		0.807 0.160 2 102343821 3 prime UTR variant C/G snv 0.21
CUI: C0085580
Disease: Essential Hypertension
Essential Hypertension 		Cardiovascular Diseases 0.010 1.000 1 2017 2017
dbSNP: rs6543116
rs6543116 		0.882 0.120 2 102311266 upstream gene variant A/G snv 0.76
CUI: C0085580
Disease: Essential Hypertension
Essential Hypertension 		Cardiovascular Diseases 0.010 1.000 1 2017 2017
dbSNP: rs1420101
rs1420101 		0.827 0.280 2 102341256 synonymous variant C/T snv 0.33 0.35
CUI: C1306759
Disease: Eosinophilic disorder
Eosinophilic disorder 		Hemic and Lymphatic Diseases 0.010 1.000 1 2010 2010
dbSNP: rs1420101
rs1420101 		0.827 0.280 2 102341256 synonymous variant C/T snv 0.33 0.35
CUI: C0014457
Disease: Eosinophilia
Eosinophilia 		Hemic and Lymphatic Diseases 0.010 1.000 1 2010 2010
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: 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: rs6543119
rs6543119 		2 102346612 intron variant A/T snv 0.36
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure 		0.700 1.000 1 2018 2018
dbSNP: rs59185885
rs59185885 		1.000 0.040 2 102327786 intron variant T/G snv 0.18
CUI: C0013595
Disease: Eczema
Eczema 		Skin and Connective Tissue Diseases 0.700 1.000 1 2019 2019