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: rs3771180
rs3771180 		1.000 0.080 2 102337157 5 prime UTR variant G/A;T snv
CUI: C0004096
Disease: Asthma
Asthma 		Respiratory Tract Diseases; Immune System Diseases 0.820 1.000 4 2011 2019
dbSNP: rs72823641
rs72823641 		0.882 0.080 2 102319699 intron variant T/A;C snv
CUI: C0004096
Disease: Asthma
Asthma 		Respiratory Tract Diseases; Immune System Diseases 0.700 1.000 3 2018 2019
dbSNP: rs72823641
rs72823641 		0.882 0.080 2 102319699 intron variant T/A;C snv
CUI: C0264408
Disease: Childhood asthma
Childhood asthma 		Respiratory Tract Diseases; Immune System Diseases 0.700 1.000 2 2019 2019
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 2 2013 2016
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: 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: 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: 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: 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: rs12479210
rs12479210 		1.000 0.080 2 102332701 intron variant C/A;T snv
CUI: C0004096
Disease: Asthma
Asthma 		Respiratory Tract Diseases; Immune System Diseases 0.700 1.000 1 2019 2019
dbSNP: rs12479210
rs12479210 		1.000 0.080 2 102332701 intron variant C/A;T snv
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction 		Immune System Diseases 0.700 1.000 1 2013 2013
dbSNP: rs13017455
rs13017455 		2 102348282 intron variant C/G;T snv
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction 		Immune System Diseases 0.700 1.000 1 2013 2013
dbSNP: rs13019081
rs13019081 		2 102334362 intron variant A/C;G;T snv
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction 		Immune System Diseases 0.700 1.000 1 2013 2013
dbSNP: rs1861245
rs1861245 		0.925 0.080 2 102350446 intron variant C/T snv
CUI: C0004096
Disease: Asthma
Asthma 		Respiratory Tract Diseases; Immune System Diseases 0.700 1.000 1 2019 2019
dbSNP: rs1861245
rs1861245 		0.925 0.080 2 102350446 intron variant C/T snv
CUI: C0264408
Disease: Childhood asthma
Childhood asthma 		Respiratory Tract Diseases; Immune System Diseases 0.700 1.000 1 2019 2019
dbSNP: rs201256810
rs201256810 		0.925 0.080 2 102348073 missense variant C/T snv
CUI: C0004096
Disease: Asthma
Asthma 		Respiratory Tract Diseases; Immune System Diseases 0.010 1.000 1 2013 2013
dbSNP: rs201256810
rs201256810 		0.925 0.080 2 102348073 missense variant C/T snv
CUI: C0085129
Disease: Bronchial Hyperreactivity
Bronchial Hyperreactivity 		Respiratory Tract Diseases 0.010 1.000 1 2013 2013
dbSNP: rs2160203
rs2160203 		1.000 0.080 2 102344364 3 prime UTR variant A/C;G snv
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction 		Immune System Diseases 0.700 1.000 1 2013 2013
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: rs3771180
rs3771180 		1.000 0.080 2 102337157 5 prime UTR variant G/A;T snv
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction 		Immune System Diseases 0.700 1.000 1 2013 2013
dbSNP: rs552531342
rs552531342 		2 102351127 intron variant -/T delins
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction 		Immune System Diseases 0.700 1.000 1 2013 2013
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: 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: rs6749114
rs6749114 		2 102351127 intron variant A/C;T snv
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction 		Immune System Diseases 0.700 1.000 1 2013 2013