TNR, tenascin R, 7143

N. diseases: 36; N. variants: 3
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs58978565
rs58978565
Entrez Id: 7143
Gene Symbol: TNR
TNR
CUI: C0271084
Disease:
Exudative age-related macular degeneration
CAGAGT 0.700 GeneticVariation GWASCAT Genome-wide analysis of disease progression in age-related macular degeneration. 29346644 2018
dbSNP: rs58978565
rs58978565
Entrez Id: 7143
Gene Symbol: TNR
TNR
CUI: C2237660
Disease:
exudative macular degeneration
CAGAGT 0.700 GeneticVariation GWASCAT Genome-wide analysis of disease progression in age-related macular degeneration. 29346644 2018
dbSNP: rs11582103
rs11582103
Entrez Id: 7143
Gene Symbol: TNR
TNR
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: rs11582103
rs11582103
Entrez Id: 7143
Gene Symbol: TNR
TNR
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: rs6692146
rs6692146
Entrez Id: 7143
Gene Symbol: TNR
TNR
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: rs58978565
rs58978565
Entrez Id: 7143
Gene Symbol: TNR
TNR
CUI: C1536085
Disease:
Geographic Atrophy
0.010 GeneticVariation BEFREE Furthermore, we detected association of rs58978565 near TNR (P = 2.3 × 10-8), rs28368872 near ATF7IP2 (P = 2.9 × 10-8) and rs142450006 near MMP9 (P = 0.0006) with progression to choroidal neovascularization but not geographic atrophy. 29346644 2018