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: rs1028166
rs1028166
Entrez Id: 55714;90768
Gene Symbol: TENM3;TENM3-AS1
TENM3;TENM3-AS1
CUI: C1319315
Disease:
Adenocarcinoma 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: rs17073715
rs17073715
Entrez Id: 55714
Gene Symbol: TENM3
TENM3
CUI: C0410702
Disease:
Adolescent idiopathic scoliosis 		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: rs17072596
rs17072596
Entrez Id: 55714;90768
Gene Symbol: TENM3;TENM3-AS1
TENM3;TENM3-AS1
CUI: C0002395
Disease:
Alzheimer's Disease 		0.700 GeneticVariation GWASDB Candidate single-nucleotide polymorphisms from a genomewide association study of Alzheimer disease. 17998437 2008
dbSNP: rs6855088
rs6855088
Entrez Id: 55714
Gene Symbol: TENM3
TENM3
CUI: C0201899
Disease:
Aspartate aminotransferase measurement 		G 0.700 GeneticVariation GWASCAT Novel genetic loci identified for the pathophysiology of childhood obesity in the Hispanic population. 23251661 2012
dbSNP: rs908084
rs908084
Entrez Id: 55714
Gene Symbol: TENM3
TENM3
CUI: C0004096
Disease:
Asthma 		A 0.700 GeneticVariation GWASCAT Genome-Wide Association Study Identifies Novel Loci Associated With Diisocyanate-Induced Occupational Asthma. 25918132 2015
dbSNP: rs28625169
rs28625169
Entrez Id: 55714
Gene Symbol: TENM3
TENM3
CUI: C0005586
Disease:
Bipolar Disorder 		T 0.700 GeneticVariation GWASCAT Genetic variants associated with response to lithium treatment in bipolar disorder: a genome-wide association study. 26806518 2016
dbSNP: rs1243762658
rs1243762658
Entrez Id: 55714
Gene Symbol: TENM3
TENM3
CUI: C0240063
Disease:
Coloboma of iris 		G 0.700 GeneticVariation CLINVAR
dbSNP: rs755000701
rs755000701
Entrez Id: 55714
Gene Symbol: TENM3
TENM3
CUI: C0240063
Disease:
Coloboma of iris 		T 0.700 GeneticVariation CLINVAR
dbSNP: rs1028166
rs1028166
Entrez Id: 55714;90768
Gene Symbol: TENM3;TENM3-AS1
TENM3;TENM3-AS1
CUI: C1837315
Disease:
COLORECTAL CANCER, SUSCEPTIBILITY TO, 1 		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: C2675481
Disease:
COLORECTAL CANCER, SUSCEPTIBILITY TO, 10 		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: C3554460
Disease:
COLORECTAL CANCER, SUSCEPTIBILITY TO, 12 		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: C2677123
Disease:
COLORECTAL CANCER, SUSCEPTIBILITY TO, 3 		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: C0009402
Disease:
Colorectal Carcinoma 		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: C0009404
Disease:
Colorectal Neoplasms 		G 0.700 GeneticVariation GWASCAT No evidence of gene-calcium interactions from genome-wide analysis of colorectal cancer risk. 25192705 2014
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
dbSNP: rs17071554
rs17071554
Entrez Id: 55714
Gene Symbol: TENM3
TENM3
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: rs17198232
rs17198232
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
dbSNP: rs17198456
rs17198456
Entrez Id: 55714
Gene Symbol: TENM3
TENM3
CUI: C0023467
Disease:
Leukemia, Myelocytic, Acute 		G 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959 2017
dbSNP: rs1836655
rs1836655
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: rs28437883
rs28437883
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: rs4861967
rs4861967
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
dbSNP: rs4861967
rs4861967
Entrez Id: 55714
Gene Symbol: TENM3
TENM3
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: rs7672826
rs7672826
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: rs7695194
rs7695194
Entrez Id: 55714
Gene Symbol: TENM3
TENM3
CUI: C0023467
Disease:
Leukemia, Myelocytic, Acute 		G 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959 2017