rs1800470, TGFB1

N. diseases: 107
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Rotator cuff syndrome
CUI: C0263912
Disease: Rotator cuff syndrome
0.010 GeneticVariation BEFREE We observed that carriers of the rare allele of both studied variants of TGFB1, as well as their G/A (rs1800470/rs1800469) haplotype, were less susceptible to RCT (p < 0.05). 31444797 2020