REL, REL proto-oncogene, NF-kB subunit, 5966

N. diseases: 90; N. variants: 5
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: rs13031237
rs13031237 		1.000 0.120 2 60908994 intron variant G/T snv 0.25
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis 		Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases 0.810 1.000 3 2009 2012
dbSNP: rs34695944
rs34695944 		1.000 0.120 2 60897715 intron variant T/C snv 0.26
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis 		Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases 0.800 1.000 4 2012 2019
dbSNP: rs13031237
rs13031237 		1.000 0.120 2 60908994 intron variant G/T snv 0.25
CUI: C0021053
Disease: Immune System Diseases
Immune System Diseases 		Immune System Diseases 0.700 1.000 1 2011 2011
dbSNP: rs13031237
rs13031237 		1.000 0.120 2 60908994 intron variant G/T snv 0.25
CUI: C0004364
Disease: Autoimmune Diseases
Autoimmune Diseases 		Immune System Diseases 0.700 1.000 1 2011 2011
dbSNP: rs6545836
rs6545836 		1.000 0.040 2 60895838 intron variant G/A snv 0.22
CUI: C0013595
Disease: Eczema
Eczema 		Skin and Connective Tissue Diseases 0.700 1.000 1 2019 2019
dbSNP: rs149627368
rs149627368 		2 60922344 missense variant T/C snv 1.5E-04 1.0E-04
CUI: C0079731
Disease: B-Cell Lymphomas
B-Cell Lymphomas 		Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases 0.010 1.000 1 2007 2007
dbSNP: rs842647
rs842647 		0.827 0.400 2 60892336 intron variant G/A snv 0.62
CUI: C0007570
Disease: Celiac Disease
Celiac Disease 		Digestive System Diseases; Nutritional and Metabolic Diseases 0.010 1.000 1 2009 2009
dbSNP: rs842647
rs842647 		0.827 0.400 2 60892336 intron variant G/A snv 0.62
CUI: C0036690
Disease: Septicemia
Septicemia 		Pathological Conditions, Signs and Symptoms; Infections 0.010 1.000 1 2015 2015
dbSNP: rs842647
rs842647 		0.827 0.400 2 60892336 intron variant G/A snv 0.62
CUI: C0037284
Disease: Skin lesion
Skin lesion 		Skin and Connective Tissue Diseases 0.010 1.000 1 2016 2016
dbSNP: rs842647
rs842647 		0.827 0.400 2 60892336 intron variant G/A snv 0.62
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		Nutritional and Metabolic Diseases; Endocrine System Diseases 0.010 1.000 1 2015 2015
dbSNP: rs842647
rs842647 		0.827 0.400 2 60892336 intron variant G/A snv 0.62
CUI: C0243026
Disease: Sepsis
Sepsis 		Pathological Conditions, Signs and Symptoms; Infections 0.010 1.000 1 2015 2015
dbSNP: rs842647
rs842647 		0.827 0.400 2 60892336 intron variant G/A snv 0.62
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Skin and Connective Tissue Diseases; Stomatognathic Diseases; Cardiovascular Diseases 0.010 1.000 1 2016 2016