Source: GWASDB

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs259919
rs259919
CUI: C1836231
Disease: HIV-1, RESISTANCE TO
HIV-1, RESISTANCE TO
0.800 GeneticVariation GWASDB Common genetic variation and the control of HIV-1 in humans. 20041166

2009

dbSNP: rs259919
rs259919
ACQUIRED IMMUNODEFICIENCY SYNDROME, PROGRESSION TO
0.800 GeneticVariation GWASDB Common genetic variation and the control of HIV-1 in humans. 20041166

2009

dbSNP: rs259919
rs259919
HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, SUSCEPTIBILITY TO
0.800 GeneticVariation GWASDB Common genetic variation and the control of HIV-1 in humans. 20041166

2009

dbSNP: rs259919
rs259919
CUI: C1836233
Disease: AIDS, PROGRESSION TO
AIDS, PROGRESSION TO
0.800 GeneticVariation GWASDB Common genetic variation and the control of HIV-1 in humans. 20041166

2009

dbSNP: rs4313034
rs4313034
CUI: C0018213
Disease: Graves Disease
Graves Disease
T 0.800 GeneticVariation GWASDB Multivariate stepwise logistic regression analysis selected rs3893464, rs4313034, rs3132613, rs4248154, rs2273017, rs9394159 and rs4713693, as markers for independent risk loci for GD. 21900946

2011

dbSNP: rs6917603
rs6917603
CUI: C0523744
Disease: Lipids measurement
Lipids measurement
0.800 GeneticVariation GWASDB Genome-wide association study identifies multiple loci influencing human serum metabolite levels. 22286219

2012

dbSNP: rs7758512
rs7758512
CUI: C1836231
Disease: HIV-1, RESISTANCE TO
HIV-1, RESISTANCE TO
0.800 GeneticVariation GWASDB Common genetic variation and the control of HIV-1 in humans. 20041166

2009

dbSNP: rs7758512
rs7758512
ACQUIRED IMMUNODEFICIENCY SYNDROME, PROGRESSION TO
0.800 GeneticVariation GWASDB Common genetic variation and the control of HIV-1 in humans. 20041166

2009

dbSNP: rs7758512
rs7758512
HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, SUSCEPTIBILITY TO
0.800 GeneticVariation GWASDB Common genetic variation and the control of HIV-1 in humans. 20041166

2009

dbSNP: rs7758512
rs7758512
CUI: C1836233
Disease: AIDS, PROGRESSION TO
AIDS, PROGRESSION TO
0.800 GeneticVariation GWASDB Common genetic variation and the control of HIV-1 in humans. 20041166

2009

dbSNP: rs16896923
rs16896923
CUI: C2931822
Disease: Nasopharyngeal carcinoma
Nasopharyngeal carcinoma
0.710 GeneticVariation GWASDB A genome-wide association study of nasopharyngeal carcinoma identifies three new susceptibility loci. 20512145

2010

dbSNP: rs166327
rs166327
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
0.700 GeneticVariation GWASDB REL, encoding a member of the NF-kappaB family of transcription factors, is a newly defined risk locus for rheumatoid arthritis. 19503088

2009

dbSNP: rs259919
rs259919
CUI: C0242379
Disease: Malignant neoplasm of lung
Malignant neoplasm of lung
0.700 GeneticVariation GWASDB Influence of common genetic variation on lung cancer risk: meta-analysis of 14 900 cases and 29 485 controls. 22899653

2012

dbSNP: rs259919
rs259919
CUI: C0152013
Disease: Adenocarcinoma of lung (disorder)
Adenocarcinoma of lung (disorder)
0.700 GeneticVariation GWASDB A genome-wide association study of lung cancer identifies a region of chromosome 5p15 associated with risk for adenocarcinoma. 19836008

2009

dbSNP: rs259940
rs259940
CUI: C0242379
Disease: Malignant neoplasm of lung
Malignant neoplasm of lung
0.700 GeneticVariation GWASDB Influence of common genetic variation on lung cancer risk: meta-analysis of 14 900 cases and 29 485 controls. 22899653

2012

dbSNP: rs259940
rs259940
CUI: C0152013
Disease: Adenocarcinoma of lung (disorder)
Adenocarcinoma of lung (disorder)
0.700 GeneticVariation GWASDB A genome-wide association study of lung cancer identifies a region of chromosome 5p15 associated with risk for adenocarcinoma. 19836008

2009

dbSNP: rs3757333
rs3757333
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 GeneticVariation GWASDB Genome-wide association study of coronary artery disease in the Japanese. 21971053

2012

dbSNP: rs3869068
rs3869068
ACQUIRED IMMUNODEFICIENCY SYNDROME, PROGRESSION TO
0.700 GeneticVariation GWASDB Common genetic variation and the control of HIV-1 in humans. 20041166

2009

dbSNP: rs3869068
rs3869068
CUI: C1836233
Disease: AIDS, PROGRESSION TO
AIDS, PROGRESSION TO
0.700 GeneticVariation GWASDB Common genetic variation and the control of HIV-1 in humans. 20041166

2009

dbSNP: rs3869068
rs3869068
HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, SUSCEPTIBILITY TO
0.700 GeneticVariation GWASDB Common genetic variation and the control of HIV-1 in humans. 20041166

2009

dbSNP: rs3869068
rs3869068
CUI: C1836231
Disease: HIV-1, RESISTANCE TO
HIV-1, RESISTANCE TO
0.700 GeneticVariation GWASDB Common genetic variation and the control of HIV-1 in humans. 20041166

2009

dbSNP: rs4313034
rs4313034
Corpuscular Hemoglobin Concentration Mean
0.700 GeneticVariation GWASDB Seventy-five genetic loci influencing the human red blood cell. 23222517

2012

dbSNP: rs4711207
rs4711207
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
0.700 GeneticVariation GWASDB REL, encoding a member of the NF-kappaB family of transcription factors, is a newly defined risk locus for rheumatoid arthritis. 19503088

2009

dbSNP: rs4711207
rs4711207
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
0.700 GeneticVariation GWASDB TRAF1-C5 as a risk locus for rheumatoid arthritis--a genomewide study. 17804836

2007

dbSNP: rs9261129
rs9261129
HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, SUSCEPTIBILITY TO
0.700 GeneticVariation GWASDB Common genetic variation and the control of HIV-1 in humans. 20041166

2009