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: rs72823641
rs72823641
0.882 0.080 2 102319699 intron variant T/A;C snv
CUI: C0741260
Disease: Adult onset asthma
Adult onset asthma
0.700 1.000 1 2019 2019
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: rs72823641
rs72823641
0.882 0.080 2 102319699 intron variant T/A;C snv
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction
Immune System Diseases 0.700 1.000 1 2018 2018
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: rs950881
rs950881
1.000 0.120 2 102316052 intron variant G/A;T snv
CUI: C2607914
Disease: Allergic rhinitis (disorder)
Allergic rhinitis (disorder)
Respiratory Tract Diseases; Immune System Diseases; Otorhinolaryngologic Diseases 0.700 1.000 1 2018 2018
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: 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: rs10208293
rs10208293
0.882 0.160 2 102349850 intron variant G/A snv 0.33
CUI: C0004096
Disease: Asthma
Asthma
Respiratory Tract Diseases; Immune System Diseases 0.700 1.000 2 2016 2019
dbSNP: rs1420101
rs1420101
0.827 0.280 2 102341256 synonymous variant C/T snv 0.33 0.35
CUI: C0004096
Disease: Asthma
Asthma
Respiratory Tract Diseases; Immune System Diseases 0.710 1.000 2 2018 2019
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 2 2011 2019
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: 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: 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: 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: rs2241116
rs2241116
1.000 0.080 2 102386805 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: 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: rs3771175
rs3771175
0.925 0.080 2 102343750 3 prime UTR variant T/A snv 0.18
CUI: C0004096
Disease: Asthma
Asthma
Respiratory Tract Diseases; Immune System Diseases 0.700 1.000 1 2019 2019
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: rs11465606
rs11465606
2 102371840 intron variant C/A snv 1.6E-02
CUI: C4268744
Disease: Atypical femoral fracture
Atypical femoral fracture
0.700 1.000 1 2019 2019
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: 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
dbSNP: rs13029918
rs13029918
2 102340831 splice region variant A/G snv 1.6E-02 1.7E-02
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement
0.700 1.000 1 2018 2018
dbSNP: rs1861246
rs1861246
2 102350323 intron variant T/C snv 0.78
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement
0.700 1.000 1 2018 2018
dbSNP: rs2001461
rs2001461
2 102390760 intron variant T/C snv 0.78
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement
0.700 1.000 1 2018 2018