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: rs3780792
rs3780792 		1.000 0.080 9 133970221 intron variant A/G snv 0.29
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		Immune System Diseases; Nervous System Diseases 0.800 1.000 1 2010 2010
dbSNP: rs10993820
rs10993820 		1.000 0.040 9 133842608 intron variant A/G snv 0.18
CUI: C0339682
Disease: Regular astigmatism - corneal
Regular astigmatism - corneal 		Eye Diseases 0.700 1.000 1 2018 2018
dbSNP: rs2519796
rs2519796 		9 133960211 intron variant G/A snv 0.65
CUI: C0018935
Disease: Hematocrit procedure
Hematocrit procedure 		0.700 1.000 1 2016 2016
dbSNP: rs2519796
rs2519796 		9 133960211 intron variant G/A snv 0.65
CUI: C0518015
Disease: Hemoglobin measurement
Hemoglobin measurement 		0.700 1.000 1 2016 2016
dbSNP: rs2789845
rs2789845 		1.000 9 133934793 intron variant C/T snv 0.80
CUI: C1836233
Disease: AIDS, PROGRESSION TO
AIDS, PROGRESSION TO 		0.700 1.000 1 2019 2019
dbSNP: rs2789845
rs2789845 		1.000 9 133934793 intron variant C/T snv 0.80
CUI: C1836231
Disease: HIV-1, RESISTANCE TO
HIV-1, RESISTANCE TO 		0.700 1.000 1 2019 2019
dbSNP: rs2789845
rs2789845 		1.000 9 133934793 intron variant C/T snv 0.80
CUI: C1836232
Disease: ACQUIRED IMMUNODEFICIENCY SYNDROME, PROGRESSION TO
ACQUIRED IMMUNODEFICIENCY SYNDROME, PROGRESSION TO 		0.700 1.000 1 2019 2019
dbSNP: rs2789845
rs2789845 		1.000 9 133934793 intron variant C/T snv 0.80
CUI: C1836230
Disease: HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, SUSCEPTIBILITY TO
HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, SUSCEPTIBILITY TO 		0.700 1.000 1 2019 2019
dbSNP: rs2789845
rs2789845 		1.000 9 133934793 intron variant C/T snv 0.80
CUI: C0376705
Disease: Viral Load result
Viral Load result 		0.700 1.000 1 2019 2019
dbSNP: rs3780786
rs3780786 		1.000 0.080 9 133950943 intron variant C/G snv 6.3E-02
CUI: C0027404
Disease: Narcolepsy
Narcolepsy 		Nervous System Diseases; Mental Disorders 0.700 1.000 1 2009 2009
dbSNP: rs2156323
rs2156323 		0.882 0.040 9 133855699 intron variant G/A snv 9.2E-02
CUI: C0017606
Disease: Primary angle-closure glaucoma
Primary angle-closure glaucoma 		Eye Diseases 0.010 < 0.001 1 2010 2010
dbSNP: rs2156323
rs2156323 		0.882 0.040 9 133855699 intron variant G/A snv 9.2E-02
CUI: C0017605
Disease: Angle Closure Glaucoma
Angle Closure Glaucoma 		Eye Diseases 0.010 < 0.001 1 2010 2010
dbSNP: rs2156323
rs2156323 		0.882 0.040 9 133855699 intron variant G/A snv 9.2E-02
CUI: C0339573
Disease: Glaucoma, Primary Open Angle
Glaucoma, Primary Open Angle 		Eye Diseases 0.010 < 0.001 1 2010 2010
dbSNP: rs602990
rs602990 		1.000 0.080 9 133778872 missense variant T/A;C snv 4.0E-06; 0.49
CUI: C0028754
Disease: Obesity
Obesity 		Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases 0.010 1.000 1 2017 2017