Source: GWASCAT

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs429150
rs429150
TNXB
CUI: C0524587
Disease: Mean Corpuscular Volume (result)
Mean Corpuscular Volume (result) 		C 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252

2016
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: 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: rs369637
rs369637
TNXB
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.700 GeneticVariation GWASCAT Meta-analysis of GWAS of over 16,000 individuals with autism spectrum disorder highlights a novel locus at 10q24.32 and a significant overlap with schizophrenia. 28540026

2017
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: rs144433536
rs144433536
TNXB
CUI: C0149782
Disease: Squamous cell carcinoma of lung
Squamous cell carcinoma of lung 		T 0.700 GeneticVariation GWASCAT Large-scale association analysis identifies new lung cancer susceptibility loci and heterogeneity in genetic susceptibility across histological subtypes. 28604730

2017
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: rs185819
rs185819
TNXB
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		C 0.700 GeneticVariation GWASCAT Novel Blood Pressure Locus and Gene Discovery Using Genome-Wide Association Study and Expression Data Sets From Blood and the Kidney. 28739976

2017
dbSNP: rs8111
rs8111
ATF6B ; TNXB
CUI: C0039263
Disease: Takayasu Arteritis
Takayasu Arteritis 		0.700 GeneticVariation GWASCAT Identification of Susceptibility Loci in IL6, RPS9/LILRB3, and an Intergenic Locus on Chromosome 21q22 in Takayasu Arteritis in a Genome-Wide Association Study. 25604533

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: 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: 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: rs2856451
rs2856451
TNXB
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure 		G 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252

2016