IL1RL1, interleukin 1 receptor like 1, 9173

N. diseases: 15; N. variants: 23
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: 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: 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: 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: 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: 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: 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: rs4988958
rs4988958
1.000 0.080 2 102351825 synonymous variant T/C snv 0.34 0.46
CUI: C0264408
Disease: Childhood asthma
Childhood asthma
Respiratory Tract Diseases; Immune System Diseases 0.700 1.000 1 2018 2018
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: 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: 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
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