TNFSF13B, TNF superfamily member 13b, 10673

N. diseases: 282; N. variants: 13
Disease: Primary Sjögren's syndrome ×
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: rs12583006
rs12583006 		0.807 0.320 13 108285104 intron variant T/A snv 0.21
CUI: C0151449
Disease: Primary Sjögren's syndrome
Primary Sjögren's syndrome 		Eye Diseases; Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases; Stomatognathic Diseases 0.010 1.000 1 2014 2014
dbSNP: rs9514828
rs9514828 		0.752 0.440 13 108269025 intron variant C/T snv 0.35
CUI: C0151449
Disease: Primary Sjögren's syndrome
Primary Sjögren's syndrome 		Eye Diseases; Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases; Stomatognathic Diseases 0.010 1.000 1 2014 2014