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: rs12191877
rs12191877 		0.851 0.120 6 31285148 intron variant C/T snv 0.12
CUI: C0033860
Disease: Psoriasis
Psoriasis 		Skin and Connective Tissue Diseases 0.830 1.000 5 2009 2015
dbSNP: rs9468925
rs9468925 		0.851 0.040 6 31291060 intron variant G/A snv 0.44
CUI: C0042900
Disease: Vitiligo
Vitiligo 		Skin and Connective Tissue Diseases 0.820 1.000 3 2010 2012
dbSNP: rs10484554
rs10484554 		0.807 0.200 6 31306778 intron variant C/T snv 0.12
CUI: C0033860
Disease: Psoriasis
Psoriasis 		Skin and Connective Tissue Diseases 0.810 1.000 4 2008 2018
dbSNP: rs2524079
rs2524079 		6 31274397 intron variant G/A snv 0.44
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure 		0.800 1.000 4 2011 2019
dbSNP: rs2247056
rs2247056 		0.882 0.160 6 31297713 intron variant T/C snv 0.80
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.800 1.000 2 2010 2018
dbSNP: rs2523608
rs2523608 		0.925 0.040 6 31354782 non coding transcript exon variant G/A snv 0.19
CUI: C1836231
Disease: HIV-1, RESISTANCE TO
HIV-1, RESISTANCE TO 		0.800 1.000 2 2009 2010
dbSNP: rs2523608
rs2523608 		0.925 0.040 6 31354782 non coding transcript exon variant G/A snv 0.19
CUI: C1836232
Disease: ACQUIRED IMMUNODEFICIENCY SYNDROME, PROGRESSION TO
ACQUIRED IMMUNODEFICIENCY SYNDROME, PROGRESSION TO 		0.800 1.000 2 2009 2010
dbSNP: rs2523608
rs2523608 		0.925 0.040 6 31354782 non coding transcript exon variant G/A snv 0.19
CUI: C1836230
Disease: HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, SUSCEPTIBILITY TO
HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, SUSCEPTIBILITY TO 		0.800 1.000 2 2009 2010
dbSNP: rs2523608
rs2523608 		0.925 0.040 6 31354782 non coding transcript exon variant G/A snv 0.19
CUI: C1836233
Disease: AIDS, PROGRESSION TO
AIDS, PROGRESSION TO 		0.800 1.000 2 2009 2010
dbSNP: rs3134792
rs3134792 		0.851 0.280 6 31344549 intron variant T/G snv 8.8E-02
CUI: C0033860
Disease: Psoriasis
Psoriasis 		Skin and Connective Tissue Diseases 0.800 1.000 2 2007 2008
dbSNP: rs3819299
rs3819299 		1.000 6 31354590 non coding transcript exon variant T/G snv 7.7E-02 2.3E-02
CUI: C0032181
Disease: Platelet Count measurement
Platelet Count measurement 		0.800 1.000 2 2011 2016
dbSNP: rs9264942
rs9264942 		0.763 0.400 6 31306603 intron variant T/C snv 0.34
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		Digestive System Diseases 0.800 1.000 2 2012 2015
dbSNP: rs9264942
rs9264942 		0.763 0.400 6 31306603 intron variant T/C snv 0.34
CUI: C1836233
Disease: AIDS, PROGRESSION TO
AIDS, PROGRESSION TO 		0.800 1.000 2 2009 2010
dbSNP: rs9264942
rs9264942 		0.763 0.400 6 31306603 intron variant T/C snv 0.34
CUI: C1836230
Disease: HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, SUSCEPTIBILITY TO
HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, SUSCEPTIBILITY TO 		0.800 1.000 2 2009 2010
dbSNP: rs9264942
rs9264942 		0.763 0.400 6 31306603 intron variant T/C snv 0.34
CUI: C1836231
Disease: HIV-1, RESISTANCE TO
HIV-1, RESISTANCE TO 		0.800 1.000 2 2009 2010
dbSNP: rs9264942
rs9264942 		0.763 0.400 6 31306603 intron variant T/C snv 0.34
CUI: C1836232
Disease: ACQUIRED IMMUNODEFICIENCY SYNDROME, PROGRESSION TO
ACQUIRED IMMUNODEFICIENCY SYNDROME, PROGRESSION TO 		0.800 1.000 2 2009 2010
dbSNP: rs10484554
rs10484554 		0.807 0.200 6 31306778 intron variant C/T snv 0.12
CUI: C0001175
Disease: Acquired Immunodeficiency Syndrome
Acquired Immunodeficiency Syndrome 		Infections; Immune System Diseases 0.800 1.000 1 2009 2009
dbSNP: rs13191343
rs13191343 		1.000 0.080 6 31273332 intron variant C/G;T snv 0.13
CUI: C0003872
Disease: Arthritis, Psoriatic
Arthritis, Psoriatic 		Skin and Connective Tissue Diseases; Musculoskeletal Diseases 0.800 1.000 1 2010 2010
dbSNP: rs2523608
rs2523608 		0.925 0.040 6 31354782 non coding transcript exon variant G/A snv 0.19
CUI: C0201910
Disease: Beta-2-microglobulin measurement
Beta-2-microglobulin measurement 		0.800 1.000 1 2013 2013
dbSNP: rs4406273
rs4406273 		0.925 0.040 6 31298313 intron variant G/A snv 8.6E-02
CUI: C0033860
Disease: Psoriasis
Psoriasis 		Skin and Connective Tissue Diseases 0.800 1.000 1 2012 2012
dbSNP: rs9264638
rs9264638 		6 31270541 intron variant G/A;C snv
CUI: C0201910
Disease: Beta-2-microglobulin measurement
Beta-2-microglobulin measurement 		0.800 1.000 1 2013 2013
dbSNP: rs9368677
rs9368677 		1.000 0.120 6 31304544 intron variant G/A snv 7.4E-02
CUI: C0011615
Disease: Dermatitis, Atopic
Dermatitis, Atopic 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Immune System Diseases 0.800 1.000 1 2012 2012
dbSNP: rs2894207
rs2894207 		0.882 0.160 6 31295974 intron variant T/C snv 0.20
CUI: C2931822
Disease: Nasopharyngeal carcinoma
Nasopharyngeal carcinoma 		Neoplasms; Stomatognathic Diseases; Otorhinolaryngologic Diseases 0.720 1.000 3 2010 2018
dbSNP: rs5010528
rs5010528 		0.827 0.240 6 31273255 intron variant A/G snv 0.15
CUI: C0014518
Disease: Toxic Epidermal Necrolysis
Toxic Epidermal Necrolysis 		Skin and Connective Tissue Diseases; Immune System Diseases; Chemically-Induced Disorders; Stomatognathic Diseases 0.720 1.000 2 2017 2018
dbSNP: rs10484554
rs10484554 		0.807 0.200 6 31306778 intron variant C/T snv 0.12
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis 		Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases 0.710 1.000 2 2009 2014