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: rs4356203
rs4356203 		0.925 0.040 11 17138601 intron variant A/G snv 0.31
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		Mental Disorders 0.800 1.000 2 2011 2014
dbSNP: rs16933829
rs16933829 		0.925 11 17094129 intron variant T/C snv 6.2E-02
CUI: C2363741
Disease: HIV-1 infection
HIV-1 infection 		0.700 1.000 1 2015 2015
dbSNP: rs16933829
rs16933829 		0.925 11 17094129 intron variant T/C snv 6.2E-02
CUI: C1836232
Disease: ACQUIRED IMMUNODEFICIENCY SYNDROME, PROGRESSION TO
ACQUIRED IMMUNODEFICIENCY SYNDROME, PROGRESSION TO 		0.700 1.000 1 2015 2015
dbSNP: rs16933829
rs16933829 		0.925 11 17094129 intron variant T/C snv 6.2E-02
CUI: C1836233
Disease: AIDS, PROGRESSION TO
AIDS, PROGRESSION TO 		0.700 1.000 1 2015 2015
dbSNP: rs16933829
rs16933829 		0.925 11 17094129 intron variant T/C snv 6.2E-02
CUI: C1836231
Disease: HIV-1, RESISTANCE TO
HIV-1, RESISTANCE TO 		0.700 1.000 1 2015 2015
dbSNP: rs16933829
rs16933829 		0.925 11 17094129 intron variant T/C snv 6.2E-02
CUI: C1836230
Disease: HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, SUSCEPTIBILITY TO
HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, SUSCEPTIBILITY TO 		0.700 1.000 1 2015 2015
dbSNP: rs2052188
rs2052188 		11 17105123 intron variant C/T snv 0.40 0.43
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs4356203
rs4356203 		0.925 0.040 11 17138601 intron variant A/G snv 0.31
CUI: C0005586
Disease: Bipolar Disorder
Bipolar Disorder 		Mental Disorders 0.700 1.000 1 2014 2014
dbSNP: rs4356203
rs4356203 		0.925 0.040 11 17138601 intron variant A/G snv 0.31
CUI: C0004936
Disease: Mental disorders
Mental disorders 		Mental Disorders 0.700 1.000 1 2014 2014
dbSNP: rs4356203
rs4356203 		0.925 0.040 11 17138601 intron variant A/G snv 0.31
CUI: C0033975
Disease: Psychotic Disorders
Psychotic Disorders 		Mental Disorders 0.700 1.000 1 2014 2014
dbSNP: rs664382
rs664382 		11 17184972 intron variant A/G;T snv
CUI: C0001948
Disease: Alcohol consumption
Alcohol consumption 		Behavior and Behavior Mechanisms 0.700 1.000 1 2018 2018
dbSNP: rs664382
rs664382 		11 17184972 intron variant A/G;T snv
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 1 2018 2018
dbSNP: rs1565272952
rs1565272952 		11 17145862 splice donor variant C/A snv
CUI: C0349588
Disease: Short stature
Short stature 		0.700 0