TNFSF15, TNF superfamily member 15, 9966

N. diseases: 143; N. variants: 11
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: rs3810936
rs3810936 		0.742 0.320 9 114790605 synonymous variant T/C snv 0.71 0.75
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		Digestive System Diseases 0.850 1.000 7 2005 2018
dbSNP: rs7848647
rs7848647 		0.732 0.320 9 114806766 upstream gene variant T/C snv 0.74
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		Digestive System Diseases 0.840 1.000 6 2005 2018
dbSNP: rs6478109
rs6478109 		0.752 0.320 9 114806486 upstream gene variant A/G snv 0.74
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		Digestive System Diseases 0.830 1.000 7 2005 2016
dbSNP: rs4979462
rs4979462 		0.790 0.240 9 114804733 intron variant C/T snv 0.13
CUI: C0008312
Disease: Primary biliary cirrhosis
Primary biliary cirrhosis 		Pathological Conditions, Signs and Symptoms; Digestive System Diseases 0.830 1.000 5 2012 2019
dbSNP: rs4263839
rs4263839 		0.807 0.160 9 114804160 intron variant A/G snv 0.75
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		Digestive System Diseases 0.830 0.750 4 2008 2014
dbSNP: rs6478108
rs6478108 		0.763 0.200 9 114796423 intron variant C/T snv 0.73
CUI: C0023343
Disease: Leprosy
Leprosy 		Infections 0.810 1.000 3 2009 2016
dbSNP: rs4246905
rs4246905 		0.716 0.400 9 114790969 missense variant T/A;C snv 0.76
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis 		Digestive System Diseases 0.800 1.000 3 2011 2015
dbSNP: rs4246905
rs4246905 		0.716 0.400 9 114790969 missense variant T/A;C snv 0.76
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases 		Digestive System Diseases 0.800 1.000 1 2012 2012
dbSNP: rs6478109
rs6478109 		0.752 0.320 9 114806486 upstream gene variant A/G snv 0.74
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases 		Digestive System Diseases 0.800 1.000 1 2008 2008
dbSNP: rs6478108
rs6478108 		0.763 0.200 9 114796423 intron variant C/T snv 0.73
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		Digestive System Diseases 0.760 1.000 8 2005 2018
dbSNP: rs7848647
rs7848647 		0.732 0.320 9 114806766 upstream gene variant T/C snv 0.74
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis 		Digestive System Diseases 0.730 1.000 4 2014 2018
dbSNP: rs4979462
rs4979462 		0.790 0.240 9 114804733 intron variant C/T snv 0.13
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		Digestive System Diseases 0.720 1.000 3 2005 2016
dbSNP: rs10114470
rs10114470 		0.882 0.080 9 114785492 3 prime UTR variant T/A;C snv
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		Digestive System Diseases 0.710 1.000 2 2013 2014
dbSNP: rs6478108
rs6478108 		0.763 0.200 9 114796423 intron variant C/T snv 0.73
CUI: C0008312
Disease: Primary biliary cirrhosis
Primary biliary cirrhosis 		Pathological Conditions, Signs and Symptoms; Digestive System Diseases 0.710 1.000 2 2012 2016
dbSNP: rs7848647
rs7848647 		0.732 0.320 9 114806766 upstream gene variant T/C snv 0.74
CUI: C0038013
Disease: Ankylosing spondylitis
Ankylosing spondylitis 		Musculoskeletal Diseases 0.710 0.500 2 2015 2016
dbSNP: rs7848647
rs7848647 		0.732 0.320 9 114806766 upstream gene variant T/C snv 0.74
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases 		Digestive System Diseases 0.710 1.000 2 2015 2018
dbSNP: rs4246905
rs4246905 		0.716 0.400 9 114790969 missense variant T/A;C snv 0.76
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		Digestive System Diseases 0.700 1.000 2 2015 2015
dbSNP: rs10114470
rs10114470 		0.882 0.080 9 114785492 3 prime UTR variant T/A;C snv
CUI: C0023343
Disease: Leprosy
Leprosy 		Infections 0.700 1.000 1 2009 2009
dbSNP: rs10117785
rs10117785 		1.000 0.040 9 114789323 3 prime UTR variant T/A snv 0.34
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		Digestive System Diseases 0.700 1.000 1 2005 2005
dbSNP: rs4246905
rs4246905 		0.716 0.400 9 114790969 missense variant T/A;C snv 0.76
CUI: C0007570
Disease: Celiac Disease
Celiac Disease 		Digestive System Diseases; Nutritional and Metabolic Diseases 0.700 1.000 1 2015 2015
dbSNP: rs4246905
rs4246905 		0.716 0.400 9 114790969 missense variant T/A;C snv 0.76
CUI: C4310768
Disease: AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 2
AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 2 		0.700 1.000 1 2015 2015
dbSNP: rs4246905
rs4246905 		0.716 0.400 9 114790969 missense variant T/A;C snv 0.76
CUI: C0920350
Disease: Autoimmune thyroiditis
Autoimmune thyroiditis 		Immune System Diseases; Endocrine System Diseases 0.700 1.000 1 2015 2015
dbSNP: rs4246905
rs4246905 		0.716 0.400 9 114790969 missense variant T/A;C snv 0.76
CUI: C3150797
Disease: AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 6
AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 6 		0.700 1.000 1 2015 2015
dbSNP: rs4246905
rs4246905 		0.716 0.400 9 114790969 missense variant T/A;C snv 0.76
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic 		Skin and Connective Tissue Diseases; Immune System Diseases 0.700 1.000 1 2015 2015
dbSNP: rs4246905
rs4246905 		0.716 0.400 9 114790969 missense variant T/A;C snv 0.76
CUI: C0038013
Disease: Ankylosing spondylitis
Ankylosing spondylitis 		Musculoskeletal Diseases 0.700 1.000 1 2015 2015