IL27, interleukin 27, 246778

N. diseases: 286; N. variants: 14
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: rs26528
rs26528 		0.807 0.200 16 28506388 intron variant T/C snv 0.43
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases 		Digestive System Diseases 0.800 1.000 2 2012 2015
dbSNP: rs4788084
rs4788084 		0.827 0.200 16 28528527 downstream gene variant C/T snv 0.36
CUI: C0011854
Disease: Diabetes Mellitus, Insulin-Dependent
Diabetes Mellitus, Insulin-Dependent 		Nutritional and Metabolic Diseases; Immune System Diseases; Endocrine System Diseases 0.800 1.000 2 2009 2011
dbSNP: rs26528
rs26528 		0.807 0.200 16 28506388 intron variant T/C snv 0.43
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis 		Digestive System Diseases 0.700 1.000 2 2015 2016
dbSNP: rs26528
rs26528 		0.807 0.200 16 28506388 intron variant T/C snv 0.43
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		Digestive System Diseases 0.700 1.000 2 2015 2016
dbSNP: rs62034325
rs62034325 		16 28527319 regulatory region variant A/G snv 0.33
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 2 2017 2018
dbSNP: rs153103
rs153103 		16 28517302 intergenic variant T/C snv 0.33
CUI: C0021704
Disease: Intelligence
Intelligence 		Behavior and Behavior Mechanisms 0.700 1.000 1 2018 2018
dbSNP: rs181206
rs181206 		0.742 0.440 16 28502082 missense variant A/G snv 0.28 0.24
CUI: C0427460
Disease: Red cell distribution width determination
Red cell distribution width determination 		0.700 1.000 1 2019 2019
dbSNP: rs181206
rs181206 		0.742 0.440 16 28502082 missense variant A/G snv 0.28 0.24
CUI: C1304746
Disease: RDW - Red blood cell distribution width result
RDW - Red blood cell distribution width result 		0.700 1.000 1 2019 2019
dbSNP: rs181209
rs181209 		16 28503533 intron variant G/T snv 0.24
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs240707
rs240707 		16 28513291 upstream gene variant C/A;G;T snv
CUI: C0021704
Disease: Intelligence
Intelligence 		Behavior and Behavior Mechanisms 0.700 1.000 1 2019 2019
dbSNP: rs26528
rs26528 		0.807 0.200 16 28506388 intron variant T/C snv 0.43
CUI: C0033860
Disease: Psoriasis
Psoriasis 		Skin and Connective Tissue Diseases 0.700 1.000 1 2016 2016
dbSNP: rs26528
rs26528 		0.807 0.200 16 28506388 intron variant T/C snv 0.43
CUI: C0008313
Disease: Cholangitis, Sclerosing
Cholangitis, Sclerosing 		Digestive System Diseases 0.700 1.000 1 2016 2016
dbSNP: rs26528
rs26528 		0.807 0.200 16 28506388 intron variant T/C snv 0.43
CUI: C0038013
Disease: Ankylosing spondylitis
Ankylosing spondylitis 		Musculoskeletal Diseases 0.700 1.000 1 2016 2016
dbSNP: rs28449958
rs28449958 		1.000 0.040 16 28517460 intergenic variant G/A;C snv
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		Digestive System Diseases 0.700 1.000 1 2017 2017
dbSNP: rs28449958
rs28449958 		1.000 0.040 16 28517460 intergenic variant G/A;C snv
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases 		Digestive System Diseases 0.700 1.000 1 2017 2017
dbSNP: rs4788084
rs4788084 		0.827 0.200 16 28528527 downstream gene variant C/T snv 0.36
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		Immune System Diseases; Nervous System Diseases 0.700 1.000 1 2011 2011
dbSNP: rs4788084
rs4788084 		0.827 0.200 16 28528527 downstream gene variant C/T snv 0.36
CUI: C1272321
Disease: Autoantibody measurement
Autoantibody measurement 		0.700 1.000 1 2011 2011
dbSNP: rs56354901
rs56354901 		1.000 0.040 16 28511823 splice region variant T/A;C snv
CUI: C0021704
Disease: Intelligence
Intelligence 		Behavior and Behavior Mechanisms 0.700 1.000 1 2018 2018
dbSNP: rs56354901
rs56354901 		1.000 0.040 16 28511823 splice region variant T/A;C snv
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		Digestive System Diseases 0.700 1.000 1 2019 2019
dbSNP: rs62034318
rs62034318 		16 28515900 upstream gene variant C/T snv 0.30
CUI: C0021704
Disease: Intelligence
Intelligence 		Behavior and Behavior Mechanisms 0.700 1.000 1 2019 2019
dbSNP: rs79046494
rs79046494 		16 28516005 upstream gene variant G/A snv 0.30
CUI: C0021704
Disease: Intelligence
Intelligence 		Behavior and Behavior Mechanisms 0.700 1.000 1 2018 2018
dbSNP: rs153109
rs153109 		0.623 0.600 16 28507775 intron variant T/C snv 0.43
CUI: C0019196
Disease: Hepatitis C
Hepatitis C 		Digestive System Diseases; Infections 0.030 1.000 3 2014 2019
dbSNP: rs153109
rs153109 		0.623 0.600 16 28507775 intron variant T/C snv 0.43
CUI: C0238463
Disease: Papillary thyroid carcinoma
Papillary thyroid carcinoma 		Neoplasms; Endocrine System Diseases 0.020 1.000 2 2015 2017
dbSNP: rs153109
rs153109 		0.623 0.600 16 28507775 intron variant T/C snv 0.43
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic 		Skin and Connective Tissue Diseases; Immune System Diseases 0.020 1.000 2 2016 2016
dbSNP: rs153109
rs153109 		0.623 0.600 16 28507775 intron variant T/C snv 0.43
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis 		Digestive System Diseases 0.020 1.000 2 2016 2017