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: rs10204137
rs10204137 		0.925 0.160 2 102351752 missense variant A/G;T snv 0.34
CUI: C0010278
Disease: Craniosynostosis
Craniosynostosis 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases 0.010 1.000 1 2009 2009
dbSNP: rs10208293
rs10208293 		0.882 0.160 2 102349850 intron variant G/A snv 0.33
CUI: C0010278
Disease: Craniosynostosis
Craniosynostosis 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases 0.010 1.000 1 2009 2009
dbSNP: rs13431828
rs13431828 		0.925 0.160 2 102338193 5 prime UTR variant C/T snv 0.18
CUI: C0010278
Disease: Craniosynostosis
Craniosynostosis 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases 0.010 1.000 1 2009 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: rs2160203
rs2160203 		1.000 0.080 2 102344364 3 prime UTR variant A/C;G snv
CUI: C0010278
Disease: Craniosynostosis
Craniosynostosis 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases 0.010 1.000 1 2009 2009
dbSNP: rs4988957
rs4988957 		1.000 0.080 2 102351615 missense variant T/C;G snv 0.34; 4.0E-06 0.46
CUI: C0010278
Disease: Craniosynostosis
Craniosynostosis 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases 0.010 1.000 1 2009 2009
dbSNP: rs10204137
rs10204137 		0.925 0.160 2 102351752 missense variant A/G;T snv 0.34
CUI: C0004096
Disease: Asthma
Asthma 		Respiratory Tract Diseases; Immune System Diseases 0.700 1.000 1 2010 2010
dbSNP: rs10206753
rs10206753 		1.000 0.080 2 102351902 missense variant T/C;G snv 0.34; 4.0E-06
CUI: C0004096
Disease: Asthma
Asthma 		Respiratory Tract Diseases; Immune System Diseases 0.700 1.000 1 2010 2010
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: rs13431828
rs13431828 		0.925 0.160 2 102338193 5 prime UTR variant C/T snv 0.18
CUI: C0004096
Disease: Asthma
Asthma 		Respiratory Tract Diseases; Immune System Diseases 0.700 1.000 2 2010 2011
dbSNP: rs10173081
rs10173081 		1.000 0.080 2 102340888 intron variant C/T snv 0.18
CUI: C0004096
Disease: Asthma
Asthma 		Respiratory Tract Diseases; Immune System Diseases 0.700 1.000 1 2011 2011
dbSNP: rs1041973
rs1041973 		1.000 0.080 2 102339008 missense variant C/A snv 0.23 0.30
CUI: C0004096
Disease: Asthma
Asthma 		Respiratory Tract Diseases; Immune System Diseases 0.010 1.000 1 2011 2011
dbSNP: rs13408569
rs13408569 		1.000 0.080 2 102338596 intron variant G/C snv 0.18
CUI: C0004096
Disease: Asthma
Asthma 		Respiratory Tract Diseases; Immune System Diseases 0.700 1.000 1 2011 2011
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 2 2011 2012
dbSNP: rs1420101
rs1420101 		0.827 0.280 2 102341256 synonymous variant C/T snv 0.33 0.35
CUI: C0006271
Disease: Bronchiolitis
Bronchiolitis 		Infections; Respiratory Tract Diseases 0.010 1.000 1 2012 2012
dbSNP: rs1921622
rs1921622 		1.000 0.080 2 102349607 intron variant G/A snv 0.42
CUI: C0006271
Disease: Bronchiolitis
Bronchiolitis 		Infections; Respiratory Tract Diseases 0.010 1.000 1 2012 2012
dbSNP: rs10173081
rs10173081 		1.000 0.080 2 102340888 intron variant C/T snv 0.18
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction 		Immune System Diseases 0.700 1.000 1 2013 2013
dbSNP: rs10192157
rs10192157 		1.000 0.080 2 102351896 missense variant C/T snv 0.34 0.46
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction 		Immune System Diseases 0.700 1.000 1 2013 2013
dbSNP: rs10197862
rs10197862 		0.925 0.120 2 102350089 intron variant A/G snv 0.18
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction 		Immune System Diseases 0.700 1.000 1 2013 2013
dbSNP: rs10206753
rs10206753 		1.000 0.080 2 102351902 missense variant T/C;G snv 0.34; 4.0E-06
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction 		Immune System Diseases 0.700 1.000 1 2013 2013
dbSNP: rs10208293
rs10208293 		0.882 0.160 2 102349850 intron variant G/A snv 0.33
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction 		Immune System Diseases 0.700 1.000 1 2013 2013
dbSNP: rs11123923
rs11123923 		2 102351384 intron variant C/A;G snv
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction 		Immune System Diseases 0.700 1.000 1 2013 2013
dbSNP: rs11685424
rs11685424 		0.925 0.040 2 102310521 upstream gene variant G/A snv 0.54
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		Cardiovascular Diseases 0.010 1.000 1 2013 2013
dbSNP: rs12469506
rs12469506 		2 102349411 intron variant C/T snv 0.22
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction 		Immune System Diseases 0.700 1.000 1 2013 2013