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: rs1265115
rs1265115
CCHCR1
0.925 0.080 6 31149298 non coding transcript exon variant C/A;T snv
CUI: C1836232
Disease: ACQUIRED IMMUNODEFICIENCY SYNDROME, PROGRESSION TO
ACQUIRED IMMUNODEFICIENCY SYNDROME, PROGRESSION TO 		0.700 1.000 1 2010 2010
dbSNP: rs1265115
rs1265115
CCHCR1
0.925 0.080 6 31149298 non coding transcript exon variant C/A;T snv
CUI: C1836233
Disease: AIDS, PROGRESSION TO
AIDS, PROGRESSION TO 		0.700 1.000 1 2010 2010
dbSNP: rs1265115
rs1265115
CCHCR1
0.925 0.080 6 31149298 non coding transcript exon variant C/A;T snv
CUI: C1836230
Disease: HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, SUSCEPTIBILITY TO
HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, SUSCEPTIBILITY TO 		0.700 1.000 1 2010 2010
dbSNP: rs1265115
rs1265115
CCHCR1
0.925 0.080 6 31149298 non coding transcript exon variant C/A;T snv
CUI: C1836231
Disease: HIV-1, RESISTANCE TO
HIV-1, RESISTANCE TO 		0.700 1.000 1 2010 2010
dbSNP: rs1265115
rs1265115
CCHCR1
0.925 0.080 6 31149298 non coding transcript exon variant C/A;T snv
CUI: C0019163
Disease: Hepatitis B
Hepatitis B 		0.700 1.000 1 2013 2013