TENM2, teneurin transmembrane protein 2, 57451

N. diseases: 44; N. variants: 33
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs172137
rs172137
Entrez Id: 57451
Gene Symbol: TENM2
TENM2
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: rs175874
rs175874
Entrez Id: 57451
Gene Symbol: TENM2
TENM2
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: rs1903110
rs1903110
Entrez Id: 57451
Gene Symbol: TENM2
TENM2
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: rs278012
rs278012
Entrez Id: 57451
Gene Symbol: TENM2
TENM2
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: rs278016
rs278016
Entrez Id: 57451
Gene Symbol: TENM2
TENM2
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: rs3101178
rs3101178
Entrez Id: 57451
Gene Symbol: TENM2
TENM2
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: rs73803919
rs73803919
Entrez Id: 57451
Gene Symbol: TENM2
TENM2
CUI: C3548479
Disease:
response to bronchodilator
A 0.700 GeneticVariation GWASCAT A genome-wide association study identifies risk loci for spirometric measures among smokers of European and African ancestry. 26634245 2015
dbSNP: rs9647570
rs9647570
Entrez Id: 57451;105377709
Gene Symbol: TENM2;LOC105377709
TENM2;LOC105377709
CUI: C1314691
Disease:
Age at menarche
G 0.700 GeneticVariation GWASCAT Parent-of-origin-specific allelic associations among 106 genomic loci for age at menarche. 25231870 2014
dbSNP: rs6885116
rs6885116
Entrez Id: 57451
Gene Symbol: TENM2
TENM2
CUI: C0600298
Disease:
Periodontosis
G 0.700 GeneticVariation GWASCAT Genome-wide association study of periodontal pathogen colonization. 22699663 2012
dbSNP: rs6885116
rs6885116
Entrez Id: 57451
Gene Symbol: TENM2
TENM2
CUI: C0031099
Disease:
Periodontitis
G 0.700 GeneticVariation GWASCAT Genome-wide association study of periodontal pathogen colonization. 22699663 2012
dbSNP: rs10045595
rs10045595
Entrez Id: 57451
Gene Symbol: TENM2
TENM2
CUI: C0027404
Disease:
Narcolepsy
0.700 GeneticVariation GWASDB Genome-wide association database developed in the Japanese Integrated Database Project. 19629137 2009
dbSNP: rs172137
rs172137
Entrez Id: 57451
Gene Symbol: TENM2
TENM2
CUI: C0027404
Disease:
Narcolepsy
0.700 GeneticVariation GWASDB Genome-wide association database developed in the Japanese Integrated Database Project. 19629137 2009