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: rs10168266
rs10168266
0.801 0.250 2 191071078 intron variant C/T snp 0.19
CUI: C1527336
Disease: Sjogren's Syndrome
Sjogren's Syndrome
Eye Diseases; Immune System Diseases; Musculoskeletal Diseases; Skin and Connective Tissue Diseases; Stomatognathic Diseases 0.700 1 2014 2014
dbSNP: rs10553577
rs10553577
1.000 0.179 2 191090464 intron variant TATA/T in-del
CUI: C1527336
Disease: Sjogren's Syndrome
Sjogren's Syndrome
Eye Diseases; Immune System Diseases; Musculoskeletal Diseases; Skin and Connective Tissue Diseases; Stomatognathic Diseases 0.700 1 2014 2014
dbSNP: rs11889341
rs11889341
0.769 0.393 2 191079016 intron variant C/T snp 0.21
CUI: C1527336
Disease: Sjogren's Syndrome
Sjogren's Syndrome
Eye Diseases; Immune System Diseases; Musculoskeletal Diseases; Skin and Connective Tissue Diseases; Stomatognathic Diseases 0.700 1 2017 2017
dbSNP: rs7574865
rs7574865
0.618 0.571 2 191099907 intron variant T/G snp 0.79
CUI: C1527336
Disease: Sjogren's Syndrome
Sjogren's Syndrome
Eye Diseases; Immune System Diseases; Musculoskeletal Diseases; Skin and Connective Tissue Diseases; Stomatognathic Diseases 0.700 1 2017 2017