TMOD1, tropomodulin 1, 7111

N. diseases: 28; N. variants: 9
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1052270
rs1052270
Entrez Id: 7111;105376168
Gene Symbol: TMOD1;LOC105376168
TMOD1;LOC105376168
CUI: C0007766
Disease:
Intracranial Aneurysm 		C 0.700 GeneticVariation GWASCAT Genomic Variations in Susceptibility to Intracranial Aneurysm in the Korean Population. 30823506 2019
dbSNP: rs10982502
rs10982502
Entrez Id: 7111
Gene Symbol: TMOD1
TMOD1
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: rs10982554
rs10982554
Entrez Id: 7111
Gene Symbol: TMOD1
TMOD1
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: rs10982622
rs10982622
Entrez Id: 7111
Gene Symbol: TMOD1
TMOD1
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: rs1330125
rs1330125
Entrez Id: 7111;105376168
Gene Symbol: TMOD1;LOC105376168
TMOD1;LOC105376168
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: rs1571567
rs1571567
Entrez Id: 7111
Gene Symbol: TMOD1
TMOD1
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: rs1571567
rs1571567
Entrez Id: 7111
Gene Symbol: TMOD1
TMOD1
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: rs6478247
rs6478247
Entrez Id: 7111
Gene Symbol: TMOD1
TMOD1
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: rs7863943
rs7863943
Entrez Id: 7111
Gene Symbol: TMOD1
TMOD1
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: rs7852462
rs7852462
Entrez Id: 7111
Gene Symbol: TMOD1
TMOD1
CUI: C0004763
Disease:
Barrett Esophagus 		C 0.700 GeneticVariation GWASCAT We identified eight new risk loci associated with either Barrett's oesophagus or oesophageal adenocarcinoma, within or near the genes CFTR (rs17451754; p=4·8 × 10<sup>-10</sup>), MSRA (rs17749155; p=5·2 × 10<sup>-10</sup>), LINC00208 and BLK (rs10108511; p=2·1 × 10<sup>-9</sup>), KHDRBS2 (rs62423175; p=3·0 × 10<sup>-9</sup>), TPPP and CEP72 (rs9918259; p=3·2 × 10<sup>-9</sup>), TMOD1 (rs7852462; p=1·5 × 10<sup>-8</sup>), SATB2 (rs139606545; p=2·0 × 10<sup>-8</sup>), and HTR3C and ABCC5 (rs9823696; p=1·6 × 10<sup>-8</sup>). 27527254 2016
dbSNP: rs7852462
rs7852462
Entrez Id: 7111
Gene Symbol: TMOD1
TMOD1
CUI: C0279628
Disease:
Adenocarcinoma Of Esophagus 		C 0.700 GeneticVariation GWASCAT We identified eight new risk loci associated with either Barrett's oesophagus or oesophageal adenocarcinoma, within or near the genes CFTR (rs17451754; p=4·8 × 10<sup>-10</sup>), MSRA (rs17749155; p=5·2 × 10<sup>-10</sup>), LINC00208 and BLK (rs10108511; p=2·1 × 10<sup>-9</sup>), KHDRBS2 (rs62423175; p=3·0 × 10<sup>-9</sup>), TPPP and CEP72 (rs9918259; p=3·2 × 10<sup>-9</sup>), TMOD1 (rs7852462; p=1·5 × 10<sup>-8</sup>), SATB2 (rs139606545; p=2·0 × 10<sup>-8</sup>), and HTR3C and ABCC5 (rs9823696; p=1·6 × 10<sup>-8</sup>). 27527254 2016