TEX41, testis expressed 41, 401014

N. diseases: 28; N. variants: 32
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs3856364
rs3856364
Entrez Id: 401014
Gene Symbol: TEX41
TEX41
CUI: C0023508
Disease:
White Blood Cell Count procedure 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs72854464
rs72854464
Entrez Id: 401014
Gene Symbol: TEX41
TEX41
CUI: C0023508
Disease:
White Blood Cell Count procedure 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs11683692
rs11683692
Entrez Id: 401014
Gene Symbol: TEX41
TEX41
CUI: C0202239
Disease:
Uric acid measurement (procedure) 		T 0.700 GeneticVariation GWASCAT Target genes, variants, tissues and transcriptional pathways influencing human serum urate levels. 31578528 2019
dbSNP: rs11691685
rs11691685
Entrez Id: 401014
Gene Symbol: TEX41
TEX41
CUI: C0009324
Disease:
Ulcerative Colitis 		0.700 GeneticVariation GWASCAT Analysis of five chronic inflammatory diseases identifies 27 new associations and highlights disease-specific patterns at shared loci. 26974007 2016
dbSNP: rs10928224
rs10928224
Entrez Id: 401014
Gene Symbol: TEX41
TEX41
CUI: C0040420
Disease:
Tonometry 		T 0.700 GeneticVariation GWASCAT Genome-wide analyses identify 68 new loci associated with intraocular pressure and improve risk prediction for primary open-angle glaucoma. 29785010 2018
dbSNP: rs10928240
rs10928240
Entrez Id: 401014;100505498
Gene Symbol: TEX41;LOC100505498
TEX41;LOC100505498
CUI: C0871470
Disease:
Systolic Pressure 		G 0.700 GeneticVariation GWASCAT Trans-ethnic association study of blood pressure determinants in over 750,000 individuals. 30578418 2019
dbSNP: rs786244
rs786244
Entrez Id: 401014
Gene Symbol: TEX41
TEX41
CUI: C0871470
Disease:
Systolic Pressure 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs10928235
rs10928235
Entrez Id: 401014
Gene Symbol: TEX41
TEX41
CUI: C0037369
Disease:
Smoking 		A 0.700 GeneticVariation GWASCAT Genome-wide association analyses of risk tolerance and risky behaviors in over 1 million individuals identify hundreds of loci and shared genetic influences. 30643258 2019
dbSNP: rs2697329
rs2697329
Entrez Id: 401014;100505498
Gene Symbol: TEX41;LOC100505498
TEX41;LOC100505498
CUI: C0037369
Disease:
Smoking 		A 0.700 GeneticVariation GWASCAT Genome-wide association analyses of risk tolerance and risky behaviors in over 1 million individuals identify hundreds of loci and shared genetic influences. 30643258 2019
dbSNP: rs6714110
rs6714110
Entrez Id: 401014;100505498
Gene Symbol: TEX41;LOC100505498
TEX41;LOC100505498
CUI: C0037369
Disease:
Smoking 		A 0.700 GeneticVariation GWASCAT Genome-wide association analyses of risk tolerance and risky behaviors in over 1 million individuals identify hundreds of loci and shared genetic influences. 30643258 2019
dbSNP: rs1830321
rs1830321
Entrez Id: 401014;100505498
Gene Symbol: TEX41;LOC100505498
TEX41;LOC100505498
CUI: C0155567
Disease:
Rheumatic aortic stenosis 		T 0.700 GeneticVariation GWASCAT Genome-wide analysis yields new loci associating with aortic valve stenosis. 29511194 2018
dbSNP: rs72854462
rs72854462
Entrez Id: 401014
Gene Symbol: TEX41
TEX41
CUI: C0014772
Disease:
Red Blood Cell Count measurement 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs11691685
rs11691685
Entrez Id: 401014
Gene Symbol: TEX41
TEX41
CUI: C0033860
Disease:
Psoriasis 		0.700 GeneticVariation GWASCAT Analysis of five chronic inflammatory diseases identifies 27 new associations and highlights disease-specific patterns at shared loci. 26974007 2016
dbSNP: rs1085639
rs1085639
Entrez Id: 401014;100505498
Gene Symbol: TEX41;LOC100505498
TEX41;LOC100505498
CUI: C0596887
Disease:
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: rs115584509
rs115584509
Entrez Id: 401014
Gene Symbol: TEX41
TEX41
CUI: C0596887
Disease:
mathematical ability 		G 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: rs1384781
rs1384781
Entrez Id: 401014
Gene Symbol: TEX41
TEX41
CUI: C0596887
Disease:
mathematical ability 		T 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: rs2256460
rs2256460
Entrez Id: 401014;100505498
Gene Symbol: TEX41;LOC100505498
TEX41;LOC100505498
CUI: C0596887
Disease:
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: rs28414958
rs28414958
Entrez Id: 401014
Gene Symbol: TEX41
TEX41
CUI: C0596887
Disease:
mathematical ability 		G 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: rs28414958
rs28414958
Entrez Id: 401014
Gene Symbol: TEX41
TEX41
CUI: C0596887
Disease:
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: rs1445300
rs1445300
Entrez Id: 401014;100505498
Gene Symbol: TEX41;LOC100505498
TEX41;LOC100505498
CUI: C0023467
Disease:
Leukemia, Myelocytic, Acute 		A 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959 2017
dbSNP: rs17409500
rs17409500
Entrez Id: 401014;100505498
Gene Symbol: TEX41;LOC100505498
TEX41;LOC100505498
CUI: C0023467
Disease:
Leukemia, Myelocytic, Acute 		A 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959 2017
dbSNP: rs967295
rs967295
Entrez Id: 401014;100505498
Gene Symbol: TEX41;LOC100505498
TEX41;LOC100505498
CUI: C0023467
Disease:
Leukemia, Myelocytic, Acute 		T 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959 2017
dbSNP: rs11681525
rs11681525
Entrez Id: 401014
Gene Symbol: TEX41
TEX41
CUI: C0021390
Disease:
Inflammatory Bowel Diseases 		0.700 GeneticVariation GWASCAT Genome-wide association study implicates immune activation of multiple integrin genes in inflammatory bowel disease. 28067908 2017
dbSNP: rs11681525
rs11681525
Entrez Id: 401014
Gene Symbol: TEX41
TEX41
CUI: C0021390
Disease:
Inflammatory Bowel Diseases 		G 0.700 GeneticVariation GWASCAT Association analyses identify 38 susceptibility loci for inflammatory bowel disease and highlight shared genetic risk across populations. 26192919 2015
dbSNP: rs2246363
rs2246363
Entrez Id: 401014;100505498
Gene Symbol: TEX41;LOC100505498
TEX41;LOC100505498
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