TGFB1, transforming growth factor beta 1, 7040

N. diseases: 1558; N. variants: 50
Disease: Familial (FPAH) ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C1611743
Disease: Familial (FPAH)
Familial (FPAH) 		0.040 GeneticVariation disease BEFREE Our findings strengthen the association of TGFB1 (rs1800472) with otosclerosis and support a relationship between RELN and familial otosclerosis only, which may explain previous variable replications. 29728750 2018
CUI: C1611743
Disease: Familial (FPAH)
Familial (FPAH) 		0.040 Biomarker disease BEFREE TGFbeta and miRNA regulation in familial and sporadic breast cancer. 28881597 2017
CUI: C1611743
Disease: Familial (FPAH)
Familial (FPAH) 		0.040 Biomarker disease BEFREE Polymorphisms and haplotype structures in genes for transforming growth factor beta1 and its receptors in familial and unselected breast cancers. 15305380 2004
CUI: C1611743
Disease: Familial (FPAH)
Familial (FPAH) 		0.040 AlteredExpression disease BEFREE The contribution of familial resemblance to variation in circulatory levels of tissue inhibitors of metalloproteinases and transforming growth factor-beta1. 14517716 2004