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: rs11640716
rs11640716 		1.000 0.040 16 50631178 intron variant T/A;G snv
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		Digestive System Diseases 0.700 1.000 1 2007 2007
dbSNP: rs117372389
rs117372389 		0.724 0.240 16 50634166 3 prime UTR variant G/T snv 1.1E-02
CUI: C0004364
Disease: Autoimmune Diseases
Autoimmune Diseases 		Immune System Diseases 0.700 1.000 1 2015 2015
dbSNP: rs117372389
rs117372389 		0.724 0.240 16 50634166 3 prime UTR variant G/T snv 1.1E-02
CUI: C4014795
Disease: AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 1
AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 1 		0.700 1.000 1 2015 2015
dbSNP: rs117372389
rs117372389 		0.724 0.240 16 50634166 3 prime UTR variant G/T snv 1.1E-02
CUI: C0920350
Disease: Autoimmune thyroiditis
Autoimmune thyroiditis 		Immune System Diseases; Endocrine System Diseases 0.700 1.000 1 2015 2015
dbSNP: rs117372389
rs117372389 		0.724 0.240 16 50634166 3 prime UTR variant G/T snv 1.1E-02
CUI: C0009447
Disease: Common Variable Immunodeficiency
Common Variable Immunodeficiency 		Immune System Diseases 0.700 1.000 1 2015 2015
dbSNP: rs117372389
rs117372389 		0.724 0.240 16 50634166 3 prime UTR variant G/T snv 1.1E-02
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis 		Digestive System Diseases 0.700 1.000 1 2015 2015
dbSNP: rs117372389
rs117372389 		0.724 0.240 16 50634166 3 prime UTR variant G/T snv 1.1E-02
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic 		Skin and Connective Tissue Diseases; Immune System Diseases 0.700 1.000 1 2015 2015
dbSNP: rs117372389
rs117372389 		0.724 0.240 16 50634166 3 prime UTR variant G/T snv 1.1E-02
CUI: C0038013
Disease: Ankylosing spondylitis
Ankylosing spondylitis 		Musculoskeletal Diseases 0.700 1.000 1 2015 2015
dbSNP: rs117372389
rs117372389 		0.724 0.240 16 50634166 3 prime UTR variant G/T snv 1.1E-02
CUI: C0033860
Disease: Psoriasis
Psoriasis 		Skin and Connective Tissue Diseases 0.700 1.000 1 2015 2015
dbSNP: rs117372389
rs117372389 		0.724 0.240 16 50634166 3 prime UTR variant G/T snv 1.1E-02
CUI: C3495559
Disease: Juvenile arthritis
Juvenile arthritis 		Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases 0.700 1.000 1 2015 2015
dbSNP: rs117372389
rs117372389 		0.724 0.240 16 50634166 3 prime UTR variant G/T snv 1.1E-02
CUI: C0011854
Disease: Diabetes Mellitus, Insulin-Dependent
Diabetes Mellitus, Insulin-Dependent 		Nutritional and Metabolic Diseases; Immune System Diseases; Endocrine System Diseases 0.700 1.000 1 2015 2015
dbSNP: rs117372389
rs117372389 		0.724 0.240 16 50634166 3 prime UTR variant G/T snv 1.1E-02
CUI: C3150797
Disease: AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 6
AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 6 		0.700 1.000 1 2015 2015
dbSNP: rs117372389
rs117372389 		0.724 0.240 16 50634166 3 prime UTR variant G/T snv 1.1E-02
CUI: C4310768
Disease: AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 2
AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 2 		0.700 1.000 1 2015 2015
dbSNP: rs117372389
rs117372389 		0.724 0.240 16 50634166 3 prime UTR variant G/T snv 1.1E-02
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		Digestive System Diseases 0.700 1.000 1 2015 2015
dbSNP: rs117372389
rs117372389 		0.724 0.240 16 50634166 3 prime UTR variant G/T snv 1.1E-02
CUI: C0007570
Disease: Celiac Disease
Celiac Disease 		Digestive System Diseases; Nutritional and Metabolic Diseases 0.700 1.000 1 2015 2015
dbSNP: rs12913
rs12913 		1.000 0.040 16 50634515 3 prime UTR variant T/C snv 0.61
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		Digestive System Diseases 0.700 1.000 1 2007 2007
dbSNP: rs12924696
rs12924696 		1.000 0.040 16 50637810 3 prime UTR variant G/A;C snv
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		Digestive System Diseases 0.700 1.000 1 2007 2007
dbSNP: rs138425259
rs138425259 		16 50629566 intron variant G/A snv 5.9E-03
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure 		0.700 1.000 1 2019 2019
dbSNP: rs1558663
rs1558663 		1.000 0.040 16 50628933 intron variant G/A snv 0.57
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		Digestive System Diseases 0.700 1.000 1 2007 2007
dbSNP: rs4785220
rs4785220 		1.000 0.040 16 50593467 intron variant T/C snv 0.77
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		Digestive System Diseases 0.700 1.000 1 2007 2007
dbSNP: rs7198686
rs7198686 		1.000 0.040 16 50632655 intron variant T/A;C snv
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		Digestive System Diseases 0.700 1.000 1 2007 2007
dbSNP: rs745230
rs745230 		1.000 0.040 16 50636271 3 prime UTR variant G/A;C;T snv
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		Digestive System Diseases 0.700 1.000 1 2007 2007
dbSNP: rs8046845
rs8046845 		1.000 0.040 16 50626853 intron variant G/A;C snv
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		Digestive System Diseases 0.700 1.000 1 2007 2007
dbSNP: rs9926095
rs9926095 		1.000 0.040 16 50645404 3 prime UTR variant A/C;T snv
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		Digestive System Diseases 0.700 1.000 1 2007 2007