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: rs6933050
rs6933050 		0.925 0.200 6 31375855 non coding transcript exon variant T/C snv 0.22
CUI: C1836233
Disease: AIDS, PROGRESSION TO
AIDS, PROGRESSION TO 		0.700 1.000 1 2009 2009
dbSNP: rs6933050
rs6933050 		0.925 0.200 6 31375855 non coding transcript exon variant T/C snv 0.22
CUI: C1836231
Disease: HIV-1, RESISTANCE TO
HIV-1, RESISTANCE TO 		0.700 1.000 1 2009 2009
dbSNP: rs6933050
rs6933050 		0.925 0.200 6 31375855 non coding transcript exon variant T/C snv 0.22
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: rs6933050
rs6933050 		0.925 0.200 6 31375855 non coding transcript exon variant T/C snv 0.22
CUI: C1836232
Disease: ACQUIRED IMMUNODEFICIENCY SYNDROME, PROGRESSION TO
ACQUIRED IMMUNODEFICIENCY SYNDROME, PROGRESSION TO 		0.700 1.000 1 2009 2009
dbSNP: rs6933050
rs6933050 		0.925 0.200 6 31375855 non coding transcript exon variant T/C snv 0.22
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome 		0.700 1.000 1 2013 2013