Source: GWASCAT

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs12153855
rs12153855
TNXB
CUI: C0011615
Disease: Dermatitis, Atopic
Dermatitis, Atopic 		T 0.800 GeneticVariation GWASCAT A genome-wide association study of atopic dermatitis identifies loci with overlapping effects on asthma and psoriasis. 23886662

2013
dbSNP: rs1150757
rs1150757
TNXB
CUI: C0027873
Disease: Neuromyelitis Optica
Neuromyelitis Optica 		A 0.700 GeneticVariation GWASCAT A whole-genome sequence study identifies genetic risk factors for neuromyelitis optica. 29769526

2018
dbSNP: rs116298992
rs116298992
TNXB
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		C 0.700 GeneticVariation GWASCAT Co-regulatory networks of human serum proteins link genetics to disease. 30072576

2018
dbSNP: rs17207986
rs17207986
TNXB
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis 		G 0.810 GeneticVariation GWASCAT Comparison of the MR-UC subjects with healthy controls confirmed the contribution of the major histocompatibility complex to severe UC (peak association: rs17207986, P = 1.4 × 10(-16)) and provided genome-wide suggestive association at the TNFSF15 (TL1A) locus (peak association: rs11554257, P = 1.4 × 10(-6)). 20848476

2010
dbSNP: rs8283
rs8283
ATF6B ; TNXB
CUI: C0577608
Disease: C4 complement assay (procedure)
C4 complement assay (procedure) 		G 0.700 GeneticVariation GWASCAT Connecting genetic risk to disease end points through the human blood plasma proteome. 28240269

2017
dbSNP: rs1150754
rs1150754
TNXB
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic 		A 0.810 GeneticVariation GWASCAT Differential genetic associations for systemic lupus erythematosus based on anti-dsDNA autoantibody production. 21408207

2011
dbSNP: rs34214527
rs34214527
TNXB
CUI: C0596887
Disease: mathematical ability
mathematical ability 		C 0.700 GeneticVariation GWASCAT Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals. 30038396

2018
dbSNP: rs204883
rs204883
TNXB
CUI: C0596887
Disease: mathematical ability
mathematical ability 		A 0.700 GeneticVariation GWASCAT Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals. 30038396

2018
dbSNP: rs1150757
rs1150757
TNXB
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic 		A 0.700 GeneticVariation GWASCAT Genetic association analyses implicate aberrant regulation of innate and adaptive immunity genes in the pathogenesis of systemic lupus erythematosus. 26502338

2015
dbSNP: rs13199524
rs13199524
TNXB
CUI: C0003872
Disease: Arthritis, Psoriatic
Arthritis, Psoriatic 		0.700 GeneticVariation GWASCAT Genetic variation at the glycosaminoglycan metabolism pathway contributes to the risk of psoriatic arthritis but not psoriasis. 30552173

2019
dbSNP: rs6937318
rs6937318
TNXB
CUI: C0149745
Disease: Oral Ulcer
Oral Ulcer 		C 0.700 GeneticVariation GWASCAT Genome wide analysis for mouth ulcers identifies associations at immune regulatory loci. 30837455

2019
dbSNP: rs3130342
rs3130342
TNXB
CUI: C0040420
Disease: Tonometry
Tonometry 		A 0.700 GeneticVariation GWASCAT Genome-wide association analyses identify new loci influencing intraocular pressure. 29617998

2018
dbSNP: rs1150757
rs1150757
TNXB
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic 		0.700 GeneticVariation GWASCAT Genome-wide association meta-analysis in Chinese and European individuals identifies ten new loci associated with systemic lupus erythematosus. 27399966

2016
dbSNP: rs1150754
rs1150754
TNXB
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		C 0.700 GeneticVariation GWASCAT Genome-Wide Association Study Detected Novel Susceptibility Genes for Schizophrenia and Shared Trans-Populations/Diseases Genetic Effect. 30285260

2019
dbSNP: rs2857009
rs2857009
TNXB
CUI: C0577608
Disease: C4 complement assay (procedure)
C4 complement assay (procedure) 		G 0.800 GeneticVariation GWASCAT Genome-wide association study for serum complement C3 and C4 levels in healthy Chinese subjects. 23028341

2012
dbSNP: rs2021783
rs2021783
TNXB
CUI: C0428883
Disease: Diastolic blood pressure
Diastolic blood pressure 		C 0.700 GeneticVariation GWASCAT Genome-wide association study in Chinese identifies novel loci for blood pressure and hypertension. 25249183

2015
dbSNP: rs2021783
rs2021783
TNXB
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		C 0.700 GeneticVariation GWASCAT Genome-wide association study in Chinese identifies novel loci for blood pressure and hypertension. 25249183

2015
dbSNP: rs2021783
rs2021783
TNXB
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		C 0.700 GeneticVariation GWASCAT Genome-wide association study in Chinese identifies novel loci for blood pressure and hypertension. 25249183

2015
dbSNP: rs3134954
rs3134954
TNXB
CUI: C0040420
Disease: Tonometry
Tonometry 		0.700 GeneticVariation GWASCAT Genome-wide association study of intraocular pressure uncovers new pathways to glaucoma. 30054594

2018
dbSNP: rs41268896
rs41268896
TNXB
CUI: C0011615
Disease: Dermatitis, Atopic
Dermatitis, Atopic 		A 0.700 GeneticVariation GWASCAT Genome-wide comparative analysis of atopic dermatitis and psoriasis gives insight into opposing genetic mechanisms. 25574825

2015
dbSNP: rs9267797
rs9267797
TNXB
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		T 0.700 GeneticVariation GWASCAT Genomic atlas of the human plasma proteome. 29875488

2018
dbSNP: rs8111
rs8111
ATF6B ; TNXB
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		T 0.700 GeneticVariation GWASCAT Genomic atlas of the human plasma proteome. 29875488

2018
dbSNP: rs41316748
rs41316748
TNXB
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		C 0.700 GeneticVariation GWASCAT Genomic atlas of the human plasma proteome. 29875488

2018
dbSNP: rs375375234
rs375375234
TNXB
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		T 0.700 GeneticVariation GWASCAT Genomic atlas of the human plasma proteome. 29875488

2018
dbSNP: rs1150753
rs1150753
TNXB
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic 		0.700 GeneticVariation GWASCAT Identification of a New Susceptibility Locus for Systemic Lupus Erythematosus on Chromosome 12 in Individuals of European Ancestry. 26316170

2016