IL1RL1, interleukin 1 receptor like 1, 9173

N. diseases: 54; N. variants: 38
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: rs10197862
rs10197862
0.923 0.107 2 102350089 intron variant A/G snp 0.18
CUI: C0004096
Disease: Asthma
Asthma
Immune System Diseases; Respiratory Tract Diseases 0.810 1.000 3 2011 2014
dbSNP: rs3771180
rs3771180
1.000 0.071 2 102337157 5 prime UTR variant G/A,T snp 0.18
CUI: C0004096
Disease: Asthma
Asthma
Immune System Diseases; Respiratory Tract Diseases 0.810 1.000 3 2011 2018
dbSNP: rs13408661
rs13408661
1.000 0.071 2 102338622 intron variant G/A snp 0.18
CUI: C0004096
Disease: Asthma
Asthma
Immune System Diseases; Respiratory Tract Diseases 0.810 1.000 2 2011 2013
dbSNP: rs950881
rs950881
2 102316052 intron variant G/A,T snp 0.18
CUI: C0020517
Disease: Hypersensitivity
Hypersensitivity
Immune System Diseases 0.800 2 2013 2017
dbSNP: rs1420101
rs1420101
0.923 0.071 2 102341256 synonymous variant C/T snp 0.33 0.36
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure
0.800 1 2009 2009
dbSNP: rs1420101
rs1420101
0.923 0.071 2 102341256 synonymous variant C/T snp 0.33 0.36
CUI: C0750879
Disease: Eosinophil count result
Eosinophil count result
0.800 1 2009 2009
dbSNP: rs13431828
rs13431828
1.000 0.071 2 102338193 5 prime UTR variant C/T snp 0.18
CUI: C0004096
Disease: Asthma
Asthma
Immune System Diseases; Respiratory Tract Diseases 0.700 2 2010 2011
dbSNP: rs10173081
rs10173081
1.000 0.071 2 102340888 intron variant C/T snp 0.18
CUI: C0004096
Disease: Asthma
Asthma
Immune System Diseases; Respiratory Tract Diseases 0.700 1 2011 2011
dbSNP: rs10173081
rs10173081
1.000 0.071 2 102340888 intron variant C/T snp 0.18
CUI: C0020517
Disease: Hypersensitivity
Hypersensitivity
Immune System Diseases 0.700 1 2013 2013
dbSNP: rs10192157
rs10192157
1.000 0.071 2 102351896 missense variant C/T snp 0.34 0.45
CUI: C0004096
Disease: Asthma
Asthma
Immune System Diseases; Respiratory Tract Diseases 0.700 1 2010 2010
dbSNP: rs10192157
rs10192157
1.000 0.071 2 102351896 missense variant C/T snp 0.34 0.45
CUI: C0020517
Disease: Hypersensitivity
Hypersensitivity
Immune System Diseases 0.700 1 2013 2013
dbSNP: rs10197862
rs10197862
0.923 0.107 2 102350089 intron variant A/G snp 0.18
CUI: C0018621
Disease: Hay fever
Hay fever
Immune System Diseases; Otorhinolaryngologic Diseases; Respiratory Tract Diseases 0.700 1 2014 2014
dbSNP: rs10197862
rs10197862
0.923 0.107 2 102350089 intron variant A/G snp 0.18
CUI: C0020517
Disease: Hypersensitivity
Hypersensitivity
Immune System Diseases 0.700 1 2013 2013
dbSNP: rs10204137
rs10204137
1.000 0.071 2 102351752 missense variant A/G,T snp 0.34 0.45
CUI: C0004096
Disease: Asthma
Asthma
Immune System Diseases; Respiratory Tract Diseases 0.700 1 2010 2010
dbSNP: rs10206753
rs10206753
1.000 0.071 2 102351902 missense variant T/C,G snp 0.34; 4.0E-06 0.45
CUI: C0004096
Disease: Asthma
Asthma
Immune System Diseases; Respiratory Tract Diseases 0.700 1 2010 2010
dbSNP: rs10206753
rs10206753
1.000 0.071 2 102351902 missense variant T/C,G snp 0.34; 4.0E-06 0.45
CUI: C0020517
Disease: Hypersensitivity
Hypersensitivity
Immune System Diseases 0.700 1 2013 2013
dbSNP: rs10208293
rs10208293
2 102349850 intron variant G/A snp 0.32
CUI: C0020517
Disease: Hypersensitivity
Hypersensitivity
Immune System Diseases 0.700 1 2013 2013
dbSNP: rs10865050
rs10865050
2 102324851 intron variant G/A snp 0.18
CUI: C0020517
Disease: Hypersensitivity
Hypersensitivity
Immune System Diseases 0.700 1 2017 2017
dbSNP: rs11123923
rs11123923
2 102351384 intron variant C/A,G snp 0.33
CUI: C0020517
Disease: Hypersensitivity
Hypersensitivity
Immune System Diseases 0.700 1 2013 2013
dbSNP: rs12469506
rs12469506
2 102349411 intron variant C/T snp 0.24
CUI: C0020517
Disease: Hypersensitivity
Hypersensitivity
Immune System Diseases 0.700 1 2013 2013
dbSNP: rs12470864
rs12470864
2 102309902 intergenic variant G/A snp 0.31
CUI: C0020517
Disease: Hypersensitivity
Hypersensitivity
Immune System Diseases 0.700 1 2017 2017
dbSNP: rs12479210
rs12479210
2 102332701 intron variant C/A,T snp 3.2E-05; 0.32
CUI: C0020517
Disease: Hypersensitivity
Hypersensitivity
Immune System Diseases 0.700 1 2013 2013
dbSNP: rs12712142
rs12712142
2 102344124 3 prime UTR variant C/A snp 0.37
CUI: C0020517
Disease: Hypersensitivity
Hypersensitivity
Immune System Diseases 0.700 1 2013 2013
dbSNP: rs13001325
rs13001325
1.000 0.036 2 102322576 intron variant C/T snp 0.32
CUI: C0020517
Disease: Hypersensitivity
Hypersensitivity
Immune System Diseases 0.700 1 2013 2013
dbSNP: rs13001325
rs13001325
1.000 0.036 2 102322576 intron variant C/T snp 0.32
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
Digestive System Diseases 0.700 1 2017 2017