TENM3, teneurin transmembrane protein 3, 55714

N. diseases: 72; N. variants: 27
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs6815916
rs6815916
Entrez Id: 55714
Gene Symbol: TENM3
TENM3
CUI: C1861172
Disease:
Venous Thromboembolism 		G 0.700 GeneticVariation GWASDB A genome-wide search for common SNP x SNP interactions on the risk of venous thrombosis. 23509962 2013
dbSNP: rs192647746
rs192647746
Entrez Id: 55714
Gene Symbol: TENM3
TENM3
CUI: C0042345
Disease:
Varicosity 		G 0.700 GeneticVariation GWASCAT Clinical and Genetic Determinants of Varicose Veins. 30566020 2018
dbSNP: rs192647746
rs192647746
Entrez Id: 55714
Gene Symbol: TENM3
TENM3
CUI: C0042345
Disease:
Varicosity 		G 0.700 GeneticVariation GWASCAT Varicose veins of lower extremities: Insights from the first large-scale genetic study. 30998689 2019
dbSNP: rs17073715
rs17073715
Entrez Id: 55714
Gene Symbol: TENM3
TENM3
CUI: C1837461
Disease:
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3 		0.700 GeneticVariation GWASCAT The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease. 30019117 2018
dbSNP: rs12510251
rs12510251
Entrez Id: 55714
Gene Symbol: TENM3
TENM3
CUI: C0036341
Disease:
Schizophrenia 		A 0.700 GeneticVariation GWASCAT Genome-wide association study of schizophrenia in Ashkenazi Jews. 26198764 2015
dbSNP: rs35751669
rs35751669
Entrez Id: 55714
Gene Symbol: TENM3
TENM3
CUI: C0036341
Disease:
Schizophrenia 		G 0.700 GeneticVariation GWASCAT Genome-Wide Association Study Detected Novel Susceptibility Genes for Schizophrenia and Shared Trans-Populations/Diseases Genetic Effect. 30285260 2019
dbSNP: rs1243762658
rs1243762658
Entrez Id: 55714
Gene Symbol: TENM3
TENM3
CUI: C1843367
Disease:
Poor school performance 		G 0.700 GeneticVariation CLINVAR
dbSNP: rs755000701
rs755000701
Entrez Id: 55714
Gene Symbol: TENM3
TENM3
CUI: C1843367
Disease:
Poor school performance 		T 0.700 GeneticVariation CLINVAR
dbSNP: rs1439283
rs1439283
Entrez Id: 55714
Gene Symbol: TENM3
TENM3
CUI: C0162701
Disease:
Polysomnography 		A 0.700 GeneticVariation GWASDB Novel genetic loci identified for the pathophysiology of childhood obesity in the Hispanic population. 23251661 2012
dbSNP: rs6855088
rs6855088
Entrez Id: 55714
Gene Symbol: TENM3
TENM3
CUI: C0162701
Disease:
Polysomnography 		G 0.700 GeneticVariation GWASDB Novel genetic loci identified for the pathophysiology of childhood obesity in the Hispanic population. 23251661 2012
dbSNP: rs138013532
rs138013532
Entrez Id: 55714
Gene Symbol: TENM3
TENM3
CUI: C0202455
Disease:
Platinum measurement 		T 0.700 GeneticVariation GWASCAT Clinical and Genome-Wide Analysis of Serum Platinum Levels after Cisplatin-Based Chemotherapy. 31296530 2019
dbSNP: rs7692395
rs7692395
Entrez Id: 55714
Gene Symbol: TENM3
TENM3
CUI: C0027051
Disease:
Myocardial Infarction 		G 0.700 GeneticVariation GWASCAT Genome-Wide Association Study for Incident Myocardial Infarction and Coronary Heart Disease in Prospective Cohort Studies: The CHARGE Consortium. 26950853 2016
dbSNP: rs7672826
rs7672826
Entrez Id: 55714
Gene Symbol: TENM3
TENM3
CUI: C0026769
Disease:
Multiple Sclerosis 		0.010 GeneticVariation BEFREE A recent genome-wide association study conducted on MS identified new biallelic markers outside the HLA (human leucocyte antigen) region involved in disease susceptibility: rs1109670 (DDEF2); rs1458175 (PDZRN4); rs1529316 and rs2049306 (CSMD1); rs16914086 (TBC1D2); rs1755289 (SH3GL2); rs1841770 (ZIC1); rs651477 (EN1); rs7607490 (TRIB2); rs397020 (C20orf46); rs908821 (SLC25A36); rs7672826 (MGC45800) and rs9523762 (GPC5). 20944657 2011
dbSNP: rs1243762658
rs1243762658
Entrez Id: 55714
Gene Symbol: TENM3
TENM3
CUI: C0026010
Disease:
Microphthalmos 		G 0.700 GeneticVariation CLINVAR
dbSNP: rs755000701
rs755000701
Entrez Id: 55714
Gene Symbol: TENM3
TENM3
CUI: C0026010
Disease:
Microphthalmos 		T 0.700 GeneticVariation CLINVAR
dbSNP: rs1243762658
rs1243762658
Entrez Id: 55714
Gene Symbol: TENM3
TENM3
CUI: C3554592
Disease:
MICROPHTHALMIA, ISOLATED, WITH COLOBOMA 9 		G 0.700 GeneticVariation CLINVAR
dbSNP: rs755000701
rs755000701
Entrez Id: 55714
Gene Symbol: TENM3
TENM3
CUI: C3554592
Disease:
MICROPHTHALMIA, ISOLATED, WITH COLOBOMA 9 		T 0.700 GeneticVariation CLINVAR
dbSNP: rs2309554
rs2309554
Entrez Id: 55714;90768
Gene Symbol: TENM3;TENM3-AS1
TENM3;TENM3-AS1
CUI: C0085437
Disease:
Meningitis, Bacterial 		A 0.700 GeneticVariation GWASCAT Joint sequencing of human and pathogen genomes reveals the genetics of pneumococcal meningitis. 31092817 2019
dbSNP: rs1028166
rs1028166
Entrez Id: 55714;90768
Gene Symbol: TENM3;TENM3-AS1
TENM3;TENM3-AS1
CUI: C0007102
Disease:
Malignant tumor of colon 		G 0.700 GeneticVariation GWASCAT No evidence of gene-calcium interactions from genome-wide analysis of colorectal cancer risk. 25192705 2014
dbSNP: rs1028166
rs1028166
Entrez Id: 55714;90768
Gene Symbol: TENM3;TENM3-AS1
TENM3;TENM3-AS1
CUI: C0346629
Disease:
Malignant neoplasm of large intestine 		G 0.700 GeneticVariation GWASCAT No evidence of gene-calcium interactions from genome-wide analysis of colorectal cancer risk. 25192705 2014
dbSNP: rs1878468
rs1878468
Entrez Id: 55714;90768
Gene Symbol: TENM3;TENM3-AS1
TENM3;TENM3-AS1
CUI: C0024530
Disease:
Malaria 		0.700 GeneticVariation GWASCAT Novel genetic polymorphisms associated with severe malaria and under selective pressure in North-eastern Tanzania. 29381699 2018
dbSNP: rs1243762658
rs1243762658
Entrez Id: 55714
Gene Symbol: TENM3
TENM3
CUI: C0042798
Disease:
Low Vision 		G 0.700 GeneticVariation CLINVAR
dbSNP: rs755000701
rs755000701
Entrez Id: 55714
Gene Symbol: TENM3
TENM3
CUI: C0042798
Disease:
Low Vision 		T 0.700 GeneticVariation CLINVAR
dbSNP: rs10866247
rs10866247
Entrez Id: 55714
Gene Symbol: TENM3
TENM3
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: rs1435495
rs1435495
Entrez Id: 55714
Gene Symbol: TENM3
TENM3
CUI: C0023467
Disease:
Leukemia, Myelocytic, Acute 		C 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959 2017