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: rs2026029
rs2026029 		0.827 0.120 13 49021195 intron variant A/G snv 0.58
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		Digestive System Diseases 0.700 1.000 1 2016 2016
dbSNP: rs2026029
rs2026029 		0.827 0.120 13 49021195 intron variant A/G snv 0.58
CUI: C0008313
Disease: Cholangitis, Sclerosing
Cholangitis, Sclerosing 		Digestive System Diseases 0.700 1.000 1 2016 2016
dbSNP: rs2026029
rs2026029 		0.827 0.120 13 49021195 intron variant A/G snv 0.58
CUI: C0038013
Disease: Ankylosing spondylitis
Ankylosing spondylitis 		Musculoskeletal Diseases 0.700 1.000 1 2016 2016
dbSNP: rs2026029
rs2026029 		0.827 0.120 13 49021195 intron variant A/G snv 0.58
CUI: C0033860
Disease: Psoriasis
Psoriasis 		Skin and Connective Tissue Diseases 0.700 1.000 1 2016 2016
dbSNP: rs2026029
rs2026029 		0.827 0.120 13 49021195 intron variant A/G snv 0.58
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis 		Digestive System Diseases 0.700 1.000 1 2016 2016
dbSNP: rs4942800
rs4942800 		13 49074810 intron variant T/C snv 0.58
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure 		0.700 1.000 1 2019 2019
dbSNP: rs6561505
rs6561505 		13 49179593 intron variant G/A snv 5.9E-02
CUI: C0392707
Disease: Atopy
Atopy 		Immune System Diseases 0.700 1.000 1 2011 2011
dbSNP: rs78871791
rs78871791 		13 49186941 intron variant A/G snv 2.6E-02
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019