IKZF3, IKAROS family zinc finger 3, 22806

N. diseases: 64; N. variants: 24
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: rs907092
rs907092
0.925 0.080 17 39766006 synonymous variant G/A snv 0.41 0.36
CUI: C0264408
Disease: Childhood asthma
Childhood asthma
Respiratory Tract Diseases; Immune System Diseases 0.700 1.000 1 2007 2007
dbSNP: rs9303277
rs9303277
0.790 0.240 17 39820216 intron variant C/T snv 0.52
CUI: C0264408
Disease: Childhood asthma
Childhood asthma
Respiratory Tract Diseases; Immune System Diseases 0.700 1.000 1 2007 2007
dbSNP: rs10445308
rs10445308
0.851 0.240 17 39781794 intron variant C/T snv 0.38
CUI: C0004096
Disease: Asthma
Asthma
Respiratory Tract Diseases; Immune System Diseases 0.700 1.000 1 2011 2011
dbSNP: rs2313430
rs2313430
0.925 0.160 17 39773563 intron variant T/C snv 0.48
CUI: C0004096
Disease: Asthma
Asthma
Respiratory Tract Diseases; Immune System Diseases 0.700 1.000 1 2011 2011
dbSNP: rs9909593
rs9909593
0.925 0.160 17 39813896 intron variant A/G snv 0.38
CUI: C0004096
Disease: Asthma
Asthma
Respiratory Tract Diseases; Immune System Diseases 0.700 1.000 1 2011 2011
dbSNP: rs907091
rs907091
0.851 0.280 17 39765489 3 prime UTR variant C/T snv 0.47
CUI: C0008312
Disease: Primary biliary cirrhosis
Primary biliary cirrhosis
Pathological Conditions, Signs and Symptoms; Digestive System Diseases 0.700 1.000 2 2012 2012
dbSNP: rs9303277
rs9303277
0.790 0.240 17 39820216 intron variant C/T snv 0.52
CUI: C0023892
Disease: Biliary cirrhosis
Biliary cirrhosis
Pathological Conditions, Signs and Symptoms; Digestive System Diseases 0.700 1.000 2 2010 2012
dbSNP: rs10445308
rs10445308
0.851 0.240 17 39781794 intron variant C/T snv 0.38
CUI: C0008312
Disease: Primary biliary cirrhosis
Primary biliary cirrhosis
Pathological Conditions, Signs and Symptoms; Digestive System Diseases 0.700 1.000 1 2012 2012
dbSNP: rs1453559
rs1453559
0.925 0.160 17 39864166 5 prime UTR variant T/C snv 0.47 0.52
CUI: C0004096
Disease: Asthma
Asthma
Respiratory Tract Diseases; Immune System Diseases 0.010 1.000 1 2012 2012
dbSNP: rs2313430
rs2313430
0.925 0.160 17 39773563 intron variant T/C snv 0.48
CUI: C0008312
Disease: Primary biliary cirrhosis
Primary biliary cirrhosis
Pathological Conditions, Signs and Symptoms; Digestive System Diseases 0.700 1.000 1 2012 2012
dbSNP: rs3816470
rs3816470
0.925 0.160 17 39829548 intron variant A/G snv 0.54
CUI: C0008312
Disease: Primary biliary cirrhosis
Primary biliary cirrhosis
Pathological Conditions, Signs and Symptoms; Digestive System Diseases 0.700 1.000 1 2012 2012
dbSNP: rs907091
rs907091
0.851 0.280 17 39765489 3 prime UTR variant C/T snv 0.47
CUI: C0014859
Disease: Esophageal Neoplasms
Esophageal Neoplasms
Digestive System Diseases; Neoplasms 0.700 1.000 1 2012 2012
dbSNP: rs9909593
rs9909593
0.925 0.160 17 39813896 intron variant A/G snv 0.38
CUI: C0008312
Disease: Primary biliary cirrhosis
Primary biliary cirrhosis
Pathological Conditions, Signs and Symptoms; Digestive System Diseases 0.700 1.000 1 2012 2012
dbSNP: rs10445308
rs10445308
0.851 0.240 17 39781794 intron variant C/T snv 0.38
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction
Immune System Diseases 0.700 1.000 1 2013 2013
dbSNP: rs3816470
rs3816470
0.925 0.160 17 39829548 intron variant A/G snv 0.54
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction
Immune System Diseases 0.700 1.000 1 2013 2013
dbSNP: rs907091
rs907091
0.851 0.280 17 39765489 3 prime UTR variant C/T snv 0.47
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction
Immune System Diseases 0.700 1.000 1 2013 2013
dbSNP: rs907092
rs907092
0.925 0.080 17 39766006 synonymous variant G/A snv 0.41 0.36
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction
Immune System Diseases 0.700 1.000 1 2013 2013
dbSNP: rs9303277
rs9303277
0.790 0.240 17 39820216 intron variant C/T snv 0.52
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction
Immune System Diseases 0.700 1.000 1 2013 2013
dbSNP: rs9303277
rs9303277
0.790 0.240 17 39820216 intron variant C/T snv 0.52
CUI: C0038013
Disease: Ankylosing spondylitis
Ankylosing spondylitis
Musculoskeletal Diseases 0.010 1.000 1 2013 2013
dbSNP: rs9635726
rs9635726
0.925 0.160 17 39863888 intron variant C/T snv 0.18
CUI: C0004096
Disease: Asthma
Asthma
Respiratory Tract Diseases; Immune System Diseases 0.010 1.000 1 2013 2013
dbSNP: rs9909593
rs9909593
0.925 0.160 17 39813896 intron variant A/G snv 0.38
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction
Immune System Diseases 0.700 1.000 1 2013 2013
dbSNP: rs12450323
rs12450323
0.925 0.120 17 39816455 intron variant G/T snv 0.18
CUI: C0004096
Disease: Asthma
Asthma
Respiratory Tract Diseases; Immune System Diseases 0.700 1.000 1 2014 2014
dbSNP: rs12450323
rs12450323
0.925 0.120 17 39816455 intron variant G/T snv 0.18
CUI: C0018621
Disease: Hay fever
Hay fever
Respiratory Tract Diseases; Immune System Diseases; Otorhinolaryngologic Diseases 0.700 1.000 1 2014 2014
dbSNP: rs907091
rs907091
0.851 0.280 17 39765489 3 prime UTR variant C/T snv 0.47
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic
Skin and Connective Tissue Diseases; Immune System Diseases 0.010 1.000 1 2014 2014
dbSNP: rs3816470
rs3816470
0.925 0.160 17 39829548 intron variant A/G snv 0.54
CUI: C0004096
Disease: Asthma
Asthma
Respiratory Tract Diseases; Immune System Diseases 0.710 1.000 2 2011 2015