Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs2523535
rs2523535 		0.851 0.200 6 31368473 intron variant A/G snv 0.32
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		0.700 1.000 1 2007 2007
dbSNP: rs2523535
rs2523535 		0.851 0.200 6 31368473 intron variant A/G snv 0.32
CUI: C1836232
Disease: ACQUIRED IMMUNODEFICIENCY SYNDROME, PROGRESSION TO
ACQUIRED IMMUNODEFICIENCY SYNDROME, PROGRESSION TO 		0.700 1.000 1 2009 2009
dbSNP: rs2523535
rs2523535 		0.851 0.200 6 31368473 intron variant A/G snv 0.32
CUI: C0011854
Disease: Diabetes Mellitus, Insulin-Dependent
Diabetes Mellitus, Insulin-Dependent 		0.700 1.000 1 2007 2007
dbSNP: rs2523535
rs2523535 		0.851 0.200 6 31368473 intron variant A/G snv 0.32
CUI: C1836231
Disease: HIV-1, RESISTANCE TO
HIV-1, RESISTANCE TO 		0.700 1.000 1 2009 2009
dbSNP: rs2523535
rs2523535 		0.851 0.200 6 31368473 intron variant A/G snv 0.32
CUI: C1836233
Disease: AIDS, PROGRESSION TO
AIDS, PROGRESSION TO 		0.700 1.000 1 2009 2009
dbSNP: rs2523535
rs2523535 		0.851 0.200 6 31368473 intron variant A/G snv 0.32
CUI: C1836230
Disease: HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, SUSCEPTIBILITY TO
HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, SUSCEPTIBILITY TO 		0.700 1.000 1 2009 2009
dbSNP: rs2523535
rs2523535 		0.851 0.200 6 31368473 intron variant A/G snv 0.32
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		0.700 1.000 1 2012 2012