TRAF6, TNF receptor associated factor 6, 7189

N. diseases: 254; N. variants: 10
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: rs540386
rs540386 		0.851 0.200 11 36503743 intron variant C/G;T snv
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis 		Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases 0.720 0.667 3 2012 2019
dbSNP: rs10501157
rs10501157 		11 36485319 3 prime UTR variant T/C snv 1.6E-02
CUI: C0037369
Disease: Smoking
Smoking 		Behavior and Behavior Mechanisms 0.700 1.000 1 2015 2015
dbSNP: rs10501157
rs10501157 		11 36485319 3 prime UTR variant T/C snv 1.6E-02
CUI: C1519383
Disease: Smoking Behaviors
Smoking Behaviors 		Behavior and Behavior Mechanisms 0.700 1.000 1 2015 2015
dbSNP: rs16928973
rs16928973 		0.925 0.160 11 36492695 intron variant C/T snv 1.2E-02
CUI: C0011881
Disease: Diabetic Nephropathy
Diabetic Nephropathy 		Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Endocrine System Diseases 0.010 1.000 1 2016 2016
dbSNP: rs16928973
rs16928973 		0.925 0.160 11 36492695 intron variant C/T snv 1.2E-02
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 2017 2017
dbSNP: rs331457
rs331457 		1.000 0.080 11 36502062 intron variant C/T snv 0.15
CUI: C0275551
Disease: Primary bacterial peritonitis
Primary bacterial peritonitis 		Digestive System Diseases; Infections 0.010 1.000 1 2017 2017
dbSNP: rs4755453
rs4755453 		0.925 0.080 11 36509094 intron variant C/A;G;T snv
CUI: C0243026
Disease: Sepsis
Sepsis 		Pathological Conditions, Signs and Symptoms; Infections 0.010 1.000 1 2012 2012
dbSNP: rs4755453
rs4755453 		0.925 0.080 11 36509094 intron variant C/A;G;T snv
CUI: C0036690
Disease: Septicemia
Septicemia 		Pathological Conditions, Signs and Symptoms; Infections 0.010 1.000 1 2012 2012
dbSNP: rs5030411
rs5030411 		1.000 0.080 11 36512203 intron variant G/A snv 0.49
CUI: C0043144
Disease: Wheezing
Wheezing 		Pathological Conditions, Signs and Symptoms 0.010 1.000 1 2014 2014
dbSNP: rs5030411
rs5030411 		1.000 0.080 11 36512203 intron variant G/A snv 0.49
CUI: C0948008
Disease: Ischemic stroke
Ischemic stroke 		Nervous System Diseases; Cardiovascular Diseases 0.010 1.000 1 2015 2015
dbSNP: rs5030416
rs5030416 		1.000 0.080 11 36510938 non coding transcript exon variant T/A;G snv
CUI: C0948008
Disease: Ischemic stroke
Ischemic stroke 		Nervous System Diseases; Cardiovascular Diseases 0.010 1.000 1 2015 2015
dbSNP: rs5030419
rs5030419 		1.000 0.080 11 36509193 intron variant G/A;C snv
CUI: C0275551
Disease: Primary bacterial peritonitis
Primary bacterial peritonitis 		Digestive System Diseases; Infections 0.010 1.000 1 2017 2017
dbSNP: rs5030437
rs5030437 		11 36503205 intron variant A/G snv 0.78
CUI: C0040034
Disease: Thrombocytopenia
Thrombocytopenia 		Hemic and Lymphatic Diseases 0.010 1.000 1 2012 2012
dbSNP: rs5030470
rs5030470 		11 36493896 intron variant A/G snv 0.12
CUI: C0040034
Disease: Thrombocytopenia
Thrombocytopenia 		Hemic and Lymphatic Diseases 0.010 1.000 1 2012 2012
dbSNP: rs540386
rs540386 		0.851 0.200 11 36503743 intron variant C/G;T snv
CUI: C0036421
Disease: Systemic Scleroderma
Systemic Scleroderma 		Skin and Connective Tissue Diseases 0.010 < 0.001 1 2012 2012
dbSNP: rs540386
rs540386 		0.851 0.200 11 36503743 intron variant C/G;T snv
CUI: C0039483
Disease: Giant Cell Arteritis
Giant Cell Arteritis 		Skin and Connective Tissue Diseases; Immune System Diseases; Nervous System Diseases; Cardiovascular Diseases 0.010 < 0.001 1 2012 2012
dbSNP: rs540386
rs540386 		0.851 0.200 11 36503743 intron variant C/G;T snv
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic 		Skin and Connective Tissue Diseases; Immune System Diseases 0.010 1.000 1 2012 2012