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: rs13001325
rs13001325
1.000 0.040 2 102322576 intron variant C/T snv 0.30
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
Digestive System Diseases 0.700 1.000 1 2017 2017
dbSNP: rs13001325
rs13001325
1.000 0.040 2 102322576 intron variant C/T snv 0.30
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases
Digestive System Diseases 0.700 1.000 1 2017 2017
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: rs6543116
rs6543116
0.882 0.120 2 102311266 upstream gene variant A/G snv 0.76
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis
Digestive System Diseases 0.010 1.000 1 2017 2017
dbSNP: rs3821204
rs3821204
0.807 0.160 2 102343821 3 prime UTR variant C/G snv 0.21
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma
Digestive System Diseases; Neoplasms 0.010 1.000 1 2019 2019
dbSNP: rs6543116
rs6543116
0.882 0.120 2 102311266 upstream gene variant A/G snv 0.76
CUI: C0677607
Disease: Hashimoto Disease
Hashimoto Disease
Endocrine System Diseases 0.010 1.000 1 2016 2016
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: 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: 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: 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: 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: 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
dbSNP: rs12470864
rs12470864
0.925 0.080 2 102309902 upstream gene variant G/A snv 0.30
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction
Immune System Diseases 0.700 1.000 1 2017 2017
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: rs12712142
rs12712142
2 102344124 3 prime UTR variant C/A snv 0.36
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction
Immune System Diseases 0.700 1.000 1 2013 2013
dbSNP: rs13001325
rs13001325
1.000 0.040 2 102322576 intron variant C/T snv 0.30
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: rs13408569
rs13408569
1.000 0.080 2 102338596 intron variant G/C snv 0.18
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction
Immune System Diseases 0.700 1.000 1 2013 2013
dbSNP: rs13408661
rs13408661
1.000 0.080 2 102338622 intron variant G/A snv 0.18
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction
Immune System Diseases 0.700 1.000 1 2013 2013