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: rs259919
rs259919
ZNRD1ASP
0.882 0.080 6 30057726 intron variant G/A snv 0.25
CUI: C1836231
Disease: HIV-1, RESISTANCE TO
HIV-1, RESISTANCE TO 		0.800 1.000 1 2009 2009
dbSNP: rs259919
rs259919
ZNRD1ASP
0.882 0.080 6 30057726 intron variant G/A snv 0.25
CUI: C1836232
Disease: ACQUIRED IMMUNODEFICIENCY SYNDROME, PROGRESSION TO
ACQUIRED IMMUNODEFICIENCY SYNDROME, PROGRESSION TO 		0.800 1.000 1 2009 2009
dbSNP: rs259919
rs259919
ZNRD1ASP
0.882 0.080 6 30057726 intron variant G/A snv 0.25
CUI: C1836230
Disease: HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, SUSCEPTIBILITY TO
HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, SUSCEPTIBILITY TO 		0.800 1.000 1 2009 2009
dbSNP: rs259919
rs259919
ZNRD1ASP
0.882 0.080 6 30057726 intron variant G/A snv 0.25
CUI: C1836233
Disease: AIDS, PROGRESSION TO
AIDS, PROGRESSION TO 		0.800 1.000 1 2009 2009
dbSNP: rs4313034
rs4313034
HLA-A ; HLA-J ; ZNRD1ASP
0.925 0.160 6 30006148 non coding transcript exon variant C/T snv 0.78
CUI: C0018213
Disease: Graves Disease
Graves Disease 		0.800 1.000 1 2011 2011
dbSNP: rs6917603
rs6917603
ZNRD1ASP
6 30049294 intron variant T/C snv 0.15
CUI: C0523744
Disease: Lipids measurement
Lipids measurement 		0.800 1.000 1 2012 2012
dbSNP: rs7758512
rs7758512
HLA-A ; ZNRD1ASP
1.000 6 30002812 intron variant T/G snv 0.17
CUI: C1836232
Disease: ACQUIRED IMMUNODEFICIENCY SYNDROME, PROGRESSION TO
ACQUIRED IMMUNODEFICIENCY SYNDROME, PROGRESSION TO 		0.800 1.000 1 2009 2009
dbSNP: rs7758512
rs7758512
HLA-A ; ZNRD1ASP
1.000 6 30002812 intron variant T/G snv 0.17
CUI: C1836231
Disease: HIV-1, RESISTANCE TO
HIV-1, RESISTANCE TO 		0.800 1.000 1 2009 2009
dbSNP: rs7758512
rs7758512
HLA-A ; ZNRD1ASP
1.000 6 30002812 intron variant T/G snv 0.17
CUI: C1836233
Disease: AIDS, PROGRESSION TO
AIDS, PROGRESSION TO 		0.800 1.000 1 2009 2009
dbSNP: rs7758512
rs7758512
HLA-A ; ZNRD1ASP
1.000 6 30002812 intron variant T/G snv 0.17
CUI: C1836230
Disease: HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, SUSCEPTIBILITY TO
HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, SUSCEPTIBILITY TO 		0.800 1.000 1 2009 2009
dbSNP: rs16896923
rs16896923
ETF1P1 ; ZNRD1ASP
1.000 0.120 6 30032910 non coding transcript exon variant T/C snv 5.0E-02
CUI: C2931822
Disease: Nasopharyngeal carcinoma
Nasopharyngeal carcinoma 		0.710 1.000 1 2010 2017
dbSNP: rs4711207
rs4711207
ZNRD1ASP
1.000 0.120 6 30037977 intron variant C/A snv 0.23
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis 		0.700 1.000 2 2007 2009
dbSNP: rs166327
rs166327
ZNRD1ASP
1.000 0.120 6 30035104 non coding transcript exon variant T/C snv 0.44
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis 		0.700 1.000 1 2009 2009
dbSNP: rs259919
rs259919
ZNRD1ASP
0.882 0.080 6 30057726 intron variant G/A snv 0.25
CUI: C0152013
Disease: Adenocarcinoma of lung (disorder)
Adenocarcinoma of lung (disorder) 		0.700 1.000 1 2009 2009
dbSNP: rs259919
rs259919
ZNRD1ASP
0.882 0.080 6 30057726 intron variant G/A snv 0.25
CUI: C0242379
Disease: Malignant neoplasm of lung
Malignant neoplasm of lung 		0.700 1.000 1 2012 2012
dbSNP: rs259940
rs259940
ZNRD1ASP
0.925 0.080 6 30044157 intron variant A/G snv 0.23
CUI: C0242379
Disease: Malignant neoplasm of lung
Malignant neoplasm of lung 		0.700 1.000 1 2012 2012
dbSNP: rs259940
rs259940
ZNRD1ASP
0.925 0.080 6 30044157 intron variant A/G snv 0.23
CUI: C0152013
Disease: Adenocarcinoma of lung (disorder)
Adenocarcinoma of lung (disorder) 		0.700 1.000 1 2009 2009
dbSNP: rs3757333
rs3757333
ZNRD1 ; ZNRD1ASP
1.000 0.040 6 30060829 non coding transcript exon variant C/A snv 9.8E-02
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		0.700 1.000 1 2012 2012
dbSNP: rs3869068
rs3869068
ZNRD1ASP
0.925 6 30036275 intron variant C/T snv 0.17
CUI: C1836232
Disease: ACQUIRED IMMUNODEFICIENCY SYNDROME, PROGRESSION TO
ACQUIRED IMMUNODEFICIENCY SYNDROME, PROGRESSION TO 		0.700 1.000 1 2009 2009
dbSNP: rs3869068
rs3869068
ZNRD1ASP
0.925 6 30036275 intron variant C/T snv 0.17
CUI: C1836231
Disease: HIV-1, RESISTANCE TO
HIV-1, RESISTANCE TO 		0.700 1.000 1 2009 2009
dbSNP: rs3869068
rs3869068
ZNRD1ASP
0.925 6 30036275 intron variant C/T snv 0.17
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: rs3869068
rs3869068
ZNRD1ASP
0.925 6 30036275 intron variant C/T snv 0.17
CUI: C1836233
Disease: AIDS, PROGRESSION TO
AIDS, PROGRESSION TO 		0.700 1.000 1 2009 2009
dbSNP: rs4313034
rs4313034
HLA-A ; HLA-J ; ZNRD1ASP
0.925 0.160 6 30006148 non coding transcript exon variant C/T snv 0.78
CUI: C4528257
Disease: Corpuscular Hemoglobin Concentration Mean
Corpuscular Hemoglobin Concentration Mean 		0.700 1.000 1 2012 2012
dbSNP: rs9261129
rs9261129
ZNRD1ASP
1.000 6 30011802 intron variant T/C snv 0.17
CUI: C1836231
Disease: HIV-1, RESISTANCE TO
HIV-1, RESISTANCE TO 		0.700 1.000 1 2009 2009
dbSNP: rs9261129
rs9261129
ZNRD1ASP
1.000 6 30011802 intron variant T/C snv 0.17
CUI: C1836233
Disease: AIDS, PROGRESSION TO
AIDS, PROGRESSION TO 		0.700 1.000 1 2009 2009