Source: GWASCAT

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1464510
rs1464510
LPP
CUI: C0042900
Disease: Vitiligo
Vitiligo 		T 0.810 GeneticVariation GWASCAT Variant of TYR and autoimmunity susceptibility loci in generalized vitiligo. 20410501

2010
dbSNP: rs13067593
rs13067593
LPP
CUI: C2699541
Disease: Cytokine Measurement
Cytokine Measurement 		G 0.800 GeneticVariation GWASCAT Genome-wide analysis of polymorphisms associated with cytokine responses in smallpox vaccine recipients. 22610502

2012
dbSNP: rs13076312
rs13076312
LPP
CUI: C0042900
Disease: Vitiligo
Vitiligo 		T 0.800 GeneticVariation GWASCAT Genome-wide association studies of autoimmune vitiligo identify 23 new risk loci and highlight key pathways and regulatory variants. 27723757

2016
dbSNP: rs13093110
rs13093110
LPP
CUI: C0018213
Disease: Graves Disease
Graves Disease 		T 0.800 GeneticVariation GWASCAT Seven newly identified loci for autoimmune thyroid disease. 22922229

2012
dbSNP: rs1464510
rs1464510
LPP
CUI: C0007570
Disease: Celiac Disease
Celiac Disease 		A 0.800 GeneticVariation GWASCAT Multiple common variants for celiac disease influencing immune gene expression. 20190752

2010
dbSNP: rs1464510
rs1464510
LPP
CUI: C0007570
Disease: Celiac Disease
Celiac Disease 		A 0.800 GeneticVariation GWASCAT Newly identified genetic risk variants for celiac disease related to the immune response. 18311140

2008
dbSNP: rs2030519
rs2030519
LPP
CUI: C0007570
Disease: Celiac Disease
Celiac Disease 		A 0.800 GeneticVariation GWASCAT Dense genotyping identifies and localizes multiple common and rare variant association signals in celiac disease. 22057235

2011
dbSNP: rs9851967
rs9851967
LPP
CUI: C0042900
Disease: Vitiligo
Vitiligo 		0.800 GeneticVariation GWASCAT Association analyses identify three susceptibility Loci for vitiligo in the Chinese Han population. 22951725

2013
dbSNP: rs9860547
rs9860547
LPP
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction 		A 0.800 GeneticVariation GWASCAT A genome-wide association meta-analysis of self-reported allergy identifies shared and allergy-specific susceptibility loci. 23817569

2013
dbSNP: rs112912841
rs112912841
LPP
CUI: C0015944
Disease: Fetal Membranes, Premature Rupture
Fetal Membranes, Premature Rupture 		G 0.700 GeneticVariation GWASCAT Variants in the fetal genome near pro-inflammatory cytokine genes on 2q13 associate with gestational duration. 31477735

2019
dbSNP: rs11707807
rs11707807
LPP
CUI: C0007137
Disease: Squamous cell carcinoma
Squamous cell carcinoma 		G 0.700 GeneticVariation GWASCAT Combined analysis of keratinocyte cancers identifies novel genome-wide loci. 31174203

2019
dbSNP: rs11715549
rs11715549
LPP
CUI: C0553723
Disease: Squamous cell carcinoma of skin
Squamous cell carcinoma of skin 		G 0.700 GeneticVariation GWASCAT Genome-wide association study identifies novel susceptibility loci for cutaneous squamous cell carcinoma. 27424798

2016
dbSNP: rs11719821
rs11719821
LPP
CUI: C0206710
Disease: Basal Cell Neoplasm
Basal Cell Neoplasm 		C 0.700 GeneticVariation GWASCAT Combined analysis of keratinocyte cancers identifies novel genome-wide loci. 31174203

2019
dbSNP: rs11719821
rs11719821
LPP
CUI: C0751676
Disease: Basal Cell Cancer
Basal Cell Cancer 		C 0.700 GeneticVariation GWASCAT Combined analysis of keratinocyte cancers identifies novel genome-wide loci. 31174203

2019
dbSNP: rs11719821
rs11719821
LPP
CUI: C0007117
Disease: Basal cell carcinoma
Basal cell carcinoma 		C 0.700 GeneticVariation GWASCAT Combined analysis of keratinocyte cancers identifies novel genome-wide loci. 31174203

2019
dbSNP: rs12634152
rs12634152
LPP
CUI: C0020676
Disease: Hypothyroidism
Hypothyroidism 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370

2019
dbSNP: rs12634152
rs12634152
LPP
CUI: C0264408
Disease: Childhood asthma
Childhood asthma 		T 0.700 GeneticVariation GWASCAT Shared and distinct genetic risk factors for childhood-onset and adult-onset asthma: genome-wide and transcriptome-wide studies. 31036433

2019
dbSNP: rs13076750
rs13076750
LPP
CUI: C0040420
Disease: Tonometry
Tonometry 		0.700 GeneticVariation GWASCAT A large multi-ethnic genome-wide association study identifies novel genetic loci for intraocular pressure. 29235454

2017
dbSNP: rs13093110
rs13093110
LPP
CUI: C0677607
Disease: Hashimoto Disease
Hashimoto Disease 		T 0.700 GeneticVariation GWASCAT Seven newly identified loci for autoimmune thyroid disease. 22922229

2012
dbSNP: rs13093110
rs13093110
LPP
CUI: C0920350
Disease: Autoimmune thyroiditis
Autoimmune thyroiditis 		T 0.700 GeneticVariation GWASCAT Seven newly identified loci for autoimmune thyroid disease. 22922229

2012
dbSNP: rs13099273
rs13099273
LPP
CUI: C0035242
Disease: Respiratory Tract Diseases
Respiratory Tract Diseases 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370

2019
dbSNP: rs13099273
rs13099273
LPP
CUI: C0004096
Disease: Asthma
Asthma 		A 0.700 GeneticVariation GWASCAT Shared genetics of asthma and mental health disorders: a large-scale genome-wide cross-trait analysis. 31619474

2019
dbSNP: rs149437411
rs149437411
LPP
CUI: C0017654
Disease: Glomerular Filtration Rate
Glomerular Filtration Rate 		0.700 GeneticVariation GWASCAT Identification of CDC42BPG as a novel susceptibility locus for hyperuricemia in a Japanese population. 29124443

2018
dbSNP: rs149437411
rs149437411
LPP
CUI: C0201976
Disease: Creatinine measurement, serum (procedure)
Creatinine measurement, serum (procedure) 		0.700 GeneticVariation GWASCAT Identification of CDC42BPG as a novel susceptibility locus for hyperuricemia in a Japanese population. 29124443

2018
dbSNP: rs150062338
rs150062338
LPP
CUI: C0243026
Disease: Sepsis
Sepsis 		T 0.700 GeneticVariation GWASCAT Genetic Factors of the Disease Course after Sepsis: A Genome-Wide Study for 28Day Mortality. 27639821

2016