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: rs8042861
rs8042861 		1.000 0.080 15 90434101 intron variant G/A;T snv
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		Immune System Diseases; Nervous System Diseases 0.710 1.000 2 2013 2016
dbSNP: rs11609
rs11609 		1.000 0.080 15 90500533 3 prime UTR variant C/G snv 0.42
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs2074585
rs2074585 		0.925 0.080 15 90466252 intron variant G/A snv 0.63 0.67
CUI: C0200641
Disease: Blood basophil count (lab test)
Blood basophil count (lab test) 		0.700 1.000 1 2016 2016
dbSNP: rs2074585
rs2074585 		0.925 0.080 15 90466252 intron variant G/A snv 0.63 0.67
CUI: C0002170
Disease: Alopecia
Alopecia 		Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases 0.700 1.000 1 2017 2017
dbSNP: rs2074585
rs2074585 		0.925 0.080 15 90466252 intron variant G/A snv 0.63 0.67
CUI: C1304746
Disease: RDW - Red blood cell distribution width result
RDW - Red blood cell distribution width result 		0.700 1.000 1 2019 2019
dbSNP: rs2074585
rs2074585 		0.925 0.080 15 90466252 intron variant G/A snv 0.63 0.67
CUI: C0013595
Disease: Eczema
Eczema 		Skin and Connective Tissue Diseases 0.700 1.000 1 2019 2019
dbSNP: rs2074585
rs2074585 		0.925 0.080 15 90466252 intron variant G/A snv 0.63 0.67
CUI: C0427460
Disease: Red cell distribution width determination
Red cell distribution width determination 		0.700 1.000 1 2019 2019
dbSNP: rs3540
rs3540 		15 90502176 3 prime UTR variant G/A snv 0.43
CUI: C0200635
Disease: Lymphocyte Count measurement
Lymphocyte Count measurement 		0.700 1.000 1 2016 2016
dbSNP: rs3540
rs3540 		15 90502176 3 prime UTR variant G/A snv 0.43
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction 		Immune System Diseases 0.700 1.000 1 2017 2017
dbSNP: rs11609
rs11609 		1.000 0.080 15 90500533 3 prime UTR variant C/G snv 0.42
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		Immune System Diseases; Nervous System Diseases 0.010 1.000 1 2016 2016
dbSNP: rs1410483989
rs1410483989 		0.925 0.120 15 90433737 missense variant A/G snv 4.0E-06 7.0E-06
CUI: C3489532
Disease: Cone-Rod Dystrophy 2
Cone-Rod Dystrophy 2 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases 0.010 1.000 1 2009 2009
dbSNP: rs1410483989
rs1410483989 		0.925 0.120 15 90433737 missense variant A/G snv 4.0E-06 7.0E-06
CUI: C0151718
Disease: Hypocholesterolemia
Hypocholesterolemia 		Nutritional and Metabolic Diseases 0.010 1.000 1 2009 2009