TNFSF15, TNF superfamily member 15, 9966

N. diseases: 143; N. variants: 11
Disease: Primary biliary cirrhosis ×
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: 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: 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: rs6478109
rs6478109 		0.752 0.320 9 114806486 upstream gene variant A/G snv 0.74
CUI: C0008312
Disease: Primary biliary cirrhosis
Primary biliary cirrhosis 		Pathological Conditions, Signs and Symptoms; Digestive System Diseases 0.010 1.000 1 2016 2016