TCF7L1, transcription factor 7 like 1, 83439

N. diseases: 39; N. variants: 6
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs62162674
rs62162674
Entrez Id: 83439
Gene Symbol: TCF7L1
TCF7L1
CUI: C0871470
Disease:
Systolic Pressure 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs6547598
rs6547598
Entrez Id: 83439
Gene Symbol: TCF7L1
TCF7L1
CUI: C0302592
Disease:
Cervix carcinoma 		A 0.700 GeneticVariation GWASCAT Genome-wide association study of cervical cancer suggests a role for ARRDC3 gene in human papillomavirus infection. 30412241 2019
dbSNP: rs6547599
rs6547599
Entrez Id: 83439
Gene Symbol: TCF7L1
TCF7L1
CUI: C0014772
Disease:
Red Blood Cell Count measurement 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs11904127
rs11904127
Entrez Id: 83439
Gene Symbol: TCF7L1
TCF7L1
CUI: C0005938
Disease:
Bone Density 		A 0.700 GeneticVariation GWASCAT Life-Course Genome-wide Association Study Meta-analysis of Total Body BMD and Assessment of Age-Specific Effects. 29304378 2018
dbSNP: rs2043230
rs2043230
Entrez Id: 83439;105374839
Gene Symbol: TCF7L1;LOC105374839
TCF7L1;LOC105374839
CUI: C0005938
Disease:
Bone Density 		A 0.700 GeneticVariation GWASCAT Life-Course Genome-wide Association Study Meta-analysis of Total Body BMD and Assessment of Age-Specific Effects. 29304378 2018
dbSNP: rs11547160
rs11547160
Entrez Id: 83439
Gene Symbol: TCF7L1
TCF7L1
CUI: C0029410
Disease:
Osteoarthritis of hip 		0.010 GeneticVariation BEFREE The TCF7L1 polymorphism rs11547160 was also associated with hip OA in the discovery set, but not in the replication set. 23864140 2013