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: rs7574865
rs7574865 		0.574 0.720 2 191099907 intron variant T/G snv 0.79
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic 		Skin and Connective Tissue Diseases; Immune System Diseases 0.900 0.967 30 2007 2017
dbSNP: rs7574865
rs7574865 		0.574 0.720 2 191099907 intron variant T/G snv 0.79
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis 		Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases 0.900 0.966 29 2007 2017
dbSNP: rs7574865
rs7574865 		0.574 0.720 2 191099907 intron variant T/G snv 0.79
CUI: C0004364
Disease: Autoimmune Diseases
Autoimmune Diseases 		Immune System Diseases 0.900 1.000 11 2008 2017
dbSNP: rs7574865
rs7574865 		0.574 0.720 2 191099907 intron variant T/G snv 0.79
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma 		Digestive System Diseases; Neoplasms 0.900 0.909 11 2013 2019
dbSNP: rs7574865
rs7574865 		0.574 0.720 2 191099907 intron variant T/G snv 0.79
CUI: C0036421
Disease: Systemic Scleroderma
Systemic Scleroderma 		Skin and Connective Tissue Diseases 0.870 0.778 9 2009 2017
dbSNP: rs7574865
rs7574865 		0.574 0.720 2 191099907 intron variant T/G snv 0.79
CUI: C0011854
Disease: Diabetes Mellitus, Insulin-Dependent
Diabetes Mellitus, Insulin-Dependent 		Nutritional and Metabolic Diseases; Immune System Diseases; Endocrine System Diseases 0.070 0.571 7 2008 2015
dbSNP: rs7574865
rs7574865 		0.574 0.720 2 191099907 intron variant T/G snv 0.79
CUI: C0151517
Disease: Complete atrioventricular block
Complete atrioventricular block 		Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.060 1.000 6 2013 2019
dbSNP: rs7582694
rs7582694 		0.763 0.400 2 191105394 intron variant C/G snv 0.77
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic 		Skin and Connective Tissue Diseases; Immune System Diseases 0.740 1.000 6 2008 2017
dbSNP: rs11889341
rs11889341 		0.732 0.480 2 191079016 intron variant C/T snv 0.21
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic 		Skin and Connective Tissue Diseases; Immune System Diseases 0.710 1.000 5 2015 2018
dbSNP: rs7574865
rs7574865 		0.574 0.720 2 191099907 intron variant T/G snv 0.79
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		Digestive System Diseases 0.050 0.800 5 2010 2015
dbSNP: rs7574865
rs7574865 		0.574 0.720 2 191099907 intron variant T/G snv 0.79
CUI: C0019163
Disease: Hepatitis B
Hepatitis B 		Digestive System Diseases; Infections 0.050 1.000 5 2015 2020
dbSNP: rs7574865
rs7574865 		0.574 0.720 2 191099907 intron variant T/G snv 0.79
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis 		Digestive System Diseases 0.040 0.750 4 2008 2015
dbSNP: rs7574865
rs7574865 		0.574 0.720 2 191099907 intron variant T/G snv 0.79
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases 		Digestive System Diseases 0.040 1.000 4 2008 2015
dbSNP: rs10181656
rs10181656 		0.763 0.360 2 191105153 intron variant G/C snv 0.79
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis 		Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases 0.820 1.000 3 2012 2017
dbSNP: rs3821236
rs3821236 		0.882 0.160 2 191038032 intron variant G/A snv 0.25
CUI: C0036421
Disease: Systemic Scleroderma
Systemic Scleroderma 		Skin and Connective Tissue Diseases 0.800 1.000 3 2010 2019
dbSNP: rs3821236
rs3821236 		0.882 0.160 2 191038032 intron variant G/A snv 0.25
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic 		Skin and Connective Tissue Diseases; Immune System Diseases 0.810 1.000 3 2008 2016
dbSNP: rs7574070
rs7574070 		1.000 0.200 2 191145762 intron variant A/C snv 0.55
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Skin and Connective Tissue Diseases; Stomatognathic Diseases; Cardiovascular Diseases 0.810 1.000 3 2012 2015
dbSNP: rs7574865
rs7574865 		0.574 0.720 2 191099907 intron variant T/G snv 0.79
CUI: C0524909
Disease: Hepatitis B, Chronic
Hepatitis B, Chronic 		Digestive System Diseases; Infections 0.030 1.000 3 2015 2019
dbSNP: rs7574865
rs7574865 		0.574 0.720 2 191099907 intron variant T/G snv 0.79
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 0.030 0.667 3 2010 2013
dbSNP: rs7574865
rs7574865 		0.574 0.720 2 191099907 intron variant T/G snv 0.79
CUI: C0008312
Disease: Primary biliary cirrhosis
Primary biliary cirrhosis 		Pathological Conditions, Signs and Symptoms; Digestive System Diseases 0.810 1.000 3 2012 2014
dbSNP: rs7601754
rs7601754 		0.882 0.160 2 191075725 intron variant G/A;T snv
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic 		Skin and Connective Tissue Diseases; Immune System Diseases 0.810 1.000 3 2010 2013
dbSNP: rs10168266
rs10168266 		0.776 0.400 2 191071078 intron variant C/T snv 0.19
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis 		Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases 0.700 1.000 2 2012 2012
dbSNP: rs10168266
rs10168266 		0.776 0.400 2 191071078 intron variant C/T snv 0.19
CUI: C0008312
Disease: Primary biliary cirrhosis
Primary biliary cirrhosis 		Pathological Conditions, Signs and Symptoms; Digestive System Diseases 0.710 1.000 2 2014 2017
dbSNP: rs10174238
rs10174238 		0.724 0.200 2 191108308 intron variant G/A snv 0.70
CUI: C0036421
Disease: Systemic Scleroderma
Systemic Scleroderma 		Skin and Connective Tissue Diseases 0.700 1.000 2 2018 2019
dbSNP: rs10181656
rs10181656 		0.763 0.360 2 191105153 intron variant G/C snv 0.79
CUI: C0003872
Disease: Arthritis, Psoriatic
Arthritis, Psoriatic 		Skin and Connective Tissue Diseases; Musculoskeletal Diseases 0.020 1.000 2 2012 2017