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: rs925255
rs925255 		0.827 0.120 2 28391927 intron variant C/T snv 0.38
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases 		Digestive System Diseases 0.800 1.000 2 2012 2017
dbSNP: rs925255
rs925255 		0.827 0.120 2 28391927 intron variant C/T snv 0.38
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		Digestive System Diseases 0.700 1.000 3 2015 2017
dbSNP: rs7562
rs7562 		2 28412873 3 prime UTR variant T/C snv 0.53
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 2 2017 2019
dbSNP: rs11677002
rs11677002 		1.000 0.120 2 28391534 intron variant T/C snv 0.39
CUI: C2607914
Disease: Allergic rhinitis (disorder)
Allergic rhinitis (disorder) 		Respiratory Tract Diseases; Immune System Diseases; Otorhinolaryngologic Diseases 0.700 1.000 1 2018 2018
dbSNP: rs11680860
rs11680860 		2 28391437 intron variant G/A snv 0.15
CUI: C0018498
Disease: Hair Color
Hair Color 		0.700 1.000 1 2018 2018
dbSNP: rs12473028
rs12473028 		2 28395294 intron variant G/A snv 0.39
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure 		0.700 1.000 1 2019 2019
dbSNP: rs2048240
rs2048240 		2 28417460 downstream gene variant C/T snv 0.53
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 1 2019 2019
dbSNP: rs2279990
rs2279990 		2 28413873 3 prime UTR variant A/G snv 0.41
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases 		Digestive System Diseases 0.700 1.000 1 2015 2015
dbSNP: rs4666070
rs4666070 		2 28401966 intron variant A/G;T snv
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs7562
rs7562 		2 28412873 3 prime UTR variant T/C snv 0.53
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction 		Immune System Diseases 0.700 1.000 1 2019 2019
dbSNP: rs7606480
rs7606480 		1.000 0.040 2 28409510 intron variant G/A snv 0.35
CUI: C0013595
Disease: Eczema
Eczema 		Skin and Connective Tissue Diseases 0.700 1.000 1 2019 2019
dbSNP: rs925255
rs925255 		0.827 0.120 2 28391927 intron variant C/T snv 0.38
CUI: C0033860
Disease: Psoriasis
Psoriasis 		Skin and Connective Tissue Diseases 0.700 1.000 1 2016 2016
dbSNP: rs925255
rs925255 		0.827 0.120 2 28391927 intron variant C/T snv 0.38
CUI: C0008313
Disease: Cholangitis, Sclerosing
Cholangitis, Sclerosing 		Digestive System Diseases 0.700 1.000 1 2016 2016
dbSNP: rs925255
rs925255 		0.827 0.120 2 28391927 intron variant C/T snv 0.38
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis 		Digestive System Diseases 0.700 1.000 1 2016 2016
dbSNP: rs925255
rs925255 		0.827 0.120 2 28391927 intron variant C/T snv 0.38
CUI: C0038013
Disease: Ankylosing spondylitis
Ankylosing spondylitis 		Musculoskeletal Diseases 0.700 1.000 1 2016 2016