Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs3780792
rs3780792
Entrez Id: 7410
Gene Symbol: VAV2
VAV2
CUI: C0026769
Disease:
Multiple Sclerosis
G 0.800 GeneticVariation GWASDB Evidence for VAV2 and ZNF433 as susceptibility genes for multiple sclerosis. 20598377 2010
dbSNP: rs3780792
rs3780792
Entrez Id: 7410
Gene Symbol: VAV2
VAV2
CUI: C0026769
Disease:
Multiple Sclerosis
G 0.800 GeneticVariation GWASCAT Evidence for VAV2 and ZNF433 as susceptibility genes for multiple sclerosis. 20598377 2010
dbSNP: rs2789845
rs2789845
Entrez Id: 7410
Gene Symbol: VAV2
VAV2
CUI: C1836230
Disease:
HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, SUSCEPTIBILITY TO
C 0.700 GeneticVariation GWASCAT Association Between Single-Nucleotide Polymorphisms in HLA Alleles and Human Immunodeficiency Virus Type 1 Viral Load in Demographically Diverse, Antiretroviral Therapy-Naive Participants From the Strategic Timing of AntiRetroviral Treatment Trial. 31219150 2019
dbSNP: rs2789845
rs2789845
Entrez Id: 7410
Gene Symbol: VAV2
VAV2
CUI: C1836232
Disease:
ACQUIRED IMMUNODEFICIENCY SYNDROME, PROGRESSION TO
C 0.700 GeneticVariation GWASCAT Association Between Single-Nucleotide Polymorphisms in HLA Alleles and Human Immunodeficiency Virus Type 1 Viral Load in Demographically Diverse, Antiretroviral Therapy-Naive Participants From the Strategic Timing of AntiRetroviral Treatment Trial. 31219150 2019
dbSNP: rs2789845
rs2789845
Entrez Id: 7410
Gene Symbol: VAV2
VAV2
CUI: C1836233
Disease:
AIDS, PROGRESSION TO
C 0.700 GeneticVariation GWASCAT Association Between Single-Nucleotide Polymorphisms in HLA Alleles and Human Immunodeficiency Virus Type 1 Viral Load in Demographically Diverse, Antiretroviral Therapy-Naive Participants From the Strategic Timing of AntiRetroviral Treatment Trial. 31219150 2019
dbSNP: rs2789845
rs2789845
Entrez Id: 7410
Gene Symbol: VAV2
VAV2
CUI: C1836231
Disease:
HIV-1, RESISTANCE TO
C 0.700 GeneticVariation GWASCAT Association Between Single-Nucleotide Polymorphisms in HLA Alleles and Human Immunodeficiency Virus Type 1 Viral Load in Demographically Diverse, Antiretroviral Therapy-Naive Participants From the Strategic Timing of AntiRetroviral Treatment Trial. 31219150 2019
dbSNP: rs2789845
rs2789845
Entrez Id: 7410
Gene Symbol: VAV2
VAV2
CUI: C0376705
Disease:
Viral Load result
C 0.700 GeneticVariation GWASCAT Association Between Single-Nucleotide Polymorphisms in HLA Alleles and Human Immunodeficiency Virus Type 1 Viral Load in Demographically Diverse, Antiretroviral Therapy-Naive Participants From the Strategic Timing of AntiRetroviral Treatment Trial. 31219150 2019
dbSNP: rs10993820
rs10993820
Entrez Id: 7410
Gene Symbol: VAV2
VAV2
CUI: C0339682
Disease:
Regular astigmatism - corneal
A 0.700 GeneticVariation GWASCAT Genome-wide association studies for corneal and refractive astigmatism in UK Biobank demonstrate a shared role for myopia susceptibility loci. 30306274 2018
dbSNP: rs2519796
rs2519796
Entrez Id: 7410
Gene Symbol: VAV2
VAV2
CUI: C0018935
Disease:
Hematocrit procedure
A 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs2519796
rs2519796
Entrez Id: 7410
Gene Symbol: VAV2
VAV2
CUI: C0518015
Disease:
Hemoglobin measurement
A 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs3780786
rs3780786
Entrez Id: 7410
Gene Symbol: VAV2
VAV2
CUI: C0027404
Disease:
Narcolepsy
0.700 GeneticVariation GWASDB Genome-wide association database developed in the Japanese Integrated Database Project. 19629137 2009
dbSNP: rs602990
rs602990
Entrez Id: 7410
Gene Symbol: VAV2
VAV2
CUI: C0028754
Disease:
Obesity
0.010 GeneticVariation BEFREE Our results show that being carrier of the T allele in VAV2 rs602990 polymorphism is associated with an increased risk of obesity, reduced levels of ankle-brachial index and diastolic blood pressure and reduced retinal artery caliber. 28157227 2017
dbSNP: rs2156323
rs2156323
Entrez Id: 7410
Gene Symbol: VAV2
VAV2
CUI: C0017605
Disease:
Angle Closure Glaucoma
0.010 GeneticVariation BEFREE The risk alleles of rs2156323 and rs2801219 in the Japanese were not associated with POAG (P = 0.533 and 0.133, respectively) and PACG (P = 0.223 and 0.394, respectively) in the Indian cohort. 20463313 2010
dbSNP: rs2156323
rs2156323
Entrez Id: 7410
Gene Symbol: VAV2
VAV2
CUI: C0017606
Disease:
Primary angle-closure glaucoma
0.010 GeneticVariation BEFREE The risk alleles of rs2156323 and rs2801219 in the Japanese were not associated with POAG (P = 0.533 and 0.133, respectively) and PACG (P = 0.223 and 0.394, respectively) in the Indian cohort. 20463313 2010
dbSNP: rs2156323
rs2156323
Entrez Id: 7410
Gene Symbol: VAV2
VAV2
CUI: C0339573
Disease:
Glaucoma, Primary Open Angle
0.010 GeneticVariation BEFREE The risk alleles of rs2156323 and rs2801219 in the Japanese were not associated with POAG (P = 0.533 and 0.133, respectively) and PACG (P = 0.223 and 0.394, respectively) in the Indian cohort. 20463313 2010