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: rs10840759
rs10840759
0.882 0.200 12 8138610 intron variant C/T snv 0.28
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 < 0.001 1 2015 2015
dbSNP: rs2377422
rs2377422
0.882 0.200 12 8128312 intron variant C/T snv 0.60
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 2015 2015