Source: GWASCAT

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121908120
rs121908120
WNT10A
CUI: C0001144
Disease: Acne Vulgaris
Acne Vulgaris 		T 0.700 GeneticVariation GWASCAT Genome-wide meta-analysis implicates mediators of hair follicle development and morphogenesis in risk for severe acne. 30542056

2018
dbSNP: rs1159268
rs1159268
CUI: C0001144
Disease: Acne Vulgaris
Acne Vulgaris 		A 0.700 GeneticVariation GWASCAT Genome-wide association study identifies three novel susceptibility loci for severe Acne vulgaris. 24927181

2014
dbSNP: rs11118336
rs11118336
LYPLAL1-AS1
CUI: C0001144
Disease: Acne Vulgaris
Acne Vulgaris 		C 0.700 GeneticVariation GWASCAT Genome-wide meta-analysis implicates mediators of hair follicle development and morphogenesis in risk for severe acne. 30542056

2018
dbSNP: rs1092479
rs1092479
CUI: C0001144
Disease: Acne Vulgaris
Acne Vulgaris 		C 0.700 GeneticVariation GWASCAT Genome-wide meta-analysis implicates mediators of hair follicle development and morphogenesis in risk for severe acne. 30542056

2018
dbSNP: rs10911268
rs10911268
CUI: C0001144
Disease: Acne Vulgaris
Acne Vulgaris 		C 0.700 GeneticVariation GWASCAT Genome-wide meta-analysis implicates mediators of hair follicle development and morphogenesis in risk for severe acne. 30542056

2018
dbSNP: rs8321
rs8321
ZNRD1
CUI: C0001175
Disease: Acquired Immunodeficiency Syndrome
Acquired Immunodeficiency Syndrome 		G 0.800 GeneticVariation GWASCAT Genomewide association study of an AIDS-nonprogression cohort emphasizes the role played by HLA genes (ANRS Genomewide Association Study 02). 19115949

2009
dbSNP: rs6467710
rs6467710
DGKI
CUI: C0001175
Disease: Acquired Immunodeficiency Syndrome
Acquired Immunodeficiency Syndrome 		0.800 GeneticVariation GWASCAT Genome-wide association study implicates PARD3B-based AIDS restriction. 21502085

2011
dbSNP: rs4118325
rs4118325
CUI: C0001175
Disease: Acquired Immunodeficiency Syndrome
Acquired Immunodeficiency Syndrome 		G 0.800 GeneticVariation GWASCAT Genomewide association study of a rapid progression cohort identifies new susceptibility alleles for AIDS (ANRS Genomewide Association Study 03). 19754311

2009
dbSNP: rs2395029
rs2395029
HCP5
CUI: C0001175
Disease: Acquired Immunodeficiency Syndrome
Acquired Immunodeficiency Syndrome 		G 0.800 GeneticVariation GWASCAT Genomewide association study of an AIDS-nonprogression cohort emphasizes the role played by HLA genes (ANRS Genomewide Association Study 02). 19115949

2009
dbSNP: rs11884476
rs11884476
PARD3B
CUI: C0001175
Disease: Acquired Immunodeficiency Syndrome
Acquired Immunodeficiency Syndrome 		0.800 GeneticVariation GWASCAT Genome-wide association study implicates PARD3B-based AIDS restriction. 21502085

2011
dbSNP: rs10484554
rs10484554
HLA-B ; LOC112267902
CUI: C0001175
Disease: Acquired Immunodeficiency Syndrome
Acquired Immunodeficiency Syndrome 		T 0.800 GeneticVariation GWASCAT Genomewide association study of an AIDS-nonprogression cohort emphasizes the role played by HLA genes (ANRS Genomewide Association Study 02). 19115949

2009
dbSNP: rs6954895
rs6954895
CUI: C0001807
Disease: Aggressive behavior
Aggressive behavior 		G 0.700 GeneticVariation GWASCAT Genome-wide association study of proneness to anger. 24489884

2014
dbSNP: rs3752433
rs3752433
PHEX ; PTCHD1-AS
CUI: C0001807
Disease: Aggressive behavior
Aggressive behavior 		A 0.700 GeneticVariation GWASCAT Genome-wide association study of proneness to anger. 24489884

2014
dbSNP: rs2844775
rs2844775
TRIM26
CUI: C0001807
Disease: Aggressive behavior
Aggressive behavior 		A 0.700 GeneticVariation GWASCAT Genome-wide association study of proneness to anger. 24489884

2014
dbSNP: rs2148710
rs2148710
FYN
CUI: C0001807
Disease: Aggressive behavior
Aggressive behavior 		T 0.700 GeneticVariation GWASCAT Genome-wide association study of proneness to anger. 24489884

2014
dbSNP: rs7996217
rs7996217
NALCN
CUI: C0001849
Disease: AIDS Dementia Complex
AIDS Dementia Complex 		T 0.700 GeneticVariation GWASCAT Genome-wide association study of neurocognitive impairment and dementia in HIV-infected adults. 22628157

2012
dbSNP: rs404005
rs404005
SLC8A1 ; SLC8A1-AS1
CUI: C0001849
Disease: AIDS Dementia Complex
AIDS Dementia Complex 		T 0.700 GeneticVariation GWASCAT Genome-wide association study of neurocognitive impairment and dementia in HIV-infected adults. 22628157

2012
dbSNP: rs17154929
rs17154929
CUI: C0001849
Disease: AIDS Dementia Complex
AIDS Dementia Complex 		T 0.700 GeneticVariation GWASCAT Genome-wide association study of neurocognitive impairment and dementia in HIV-infected adults. 22628157

2012
dbSNP: rs12742923
rs12742923
LINC01362 ; LOC107985037
CUI: C0001849
Disease: AIDS Dementia Complex
AIDS Dementia Complex 		T 0.700 GeneticVariation GWASCAT Genome-wide association study of neurocognitive impairment and dementia in HIV-infected adults. 22628157

2012
dbSNP: rs1801239
rs1801239
CUBN
CUI: C0001925
Disease: Albuminuria
Albuminuria 		C 0.800 GeneticVariation GWASCAT Identification of 22 novel loci associated with urinary biomarkers of albumin, sodium, and potassium excretion. 30910378

2019
dbSNP: rs1801239
rs1801239
CUBN
CUI: C0001925
Disease: Albuminuria
Albuminuria 		T 0.800 GeneticVariation GWASCAT CUBN is a gene locus for albuminuria. 21355061

2011
dbSNP: rs838142
rs838142
FUT1 ; IZUMO1
CUI: C0001925
Disease: Albuminuria
Albuminuria 		A 0.700 GeneticVariation GWASCAT Genetic Association of Albuminuria with Cardiometabolic Disease and Blood Pressure. 30220432

2018
dbSNP: rs8035855
rs8035855
MAPKBP1
CUI: C0001925
Disease: Albuminuria
Albuminuria 		A 0.700 GeneticVariation GWASCAT Genetic Association of Albuminuria with Cardiometabolic Disease and Blood Pressure. 30220432

2018
dbSNP: rs784257
rs784257
LOC105372130
CUI: C0001925
Disease: Albuminuria
Albuminuria 		T 0.700 GeneticVariation GWASCAT Genetic Association of Albuminuria with Cardiometabolic Disease and Blood Pressure. 30220432

2018
dbSNP: rs7731168
rs7731168
CWC27
CUI: C0001925
Disease: Albuminuria
Albuminuria 		C 0.700 GeneticVariation GWASCAT Genetic Association of Albuminuria with Cardiometabolic Disease and Blood Pressure. 30220432

2018