rs76992529, TTR

N. diseases: 36
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Heart failure
CUI: C0018801
Disease: Heart failure
0.060 GeneticVariation BEFREE Among individuals of African or Hispanic/Latino ancestry enrolled in 2 academic medical center-based biobanks, the TTR V122I genetic variant was significantly associated with heart failure. 31821430 2019
Heart failure
CUI: C0018801
Disease: Heart failure
0.060 GeneticVariation BEFREE This clinical algorithm may be useful for identification of ATTR V122I amyloidosis in elderly African American patients with HF. 28196196 2017
Heart failure
CUI: C0018801
Disease: Heart failure
0.060 GeneticVariation BEFREE Patients with ATTR V122I had the worst prognosis compared with other causes of Afro-Caribbean heart failure and white patients. 27618855 2016
Heart failure
CUI: C0018801
Disease: Heart failure
0.060 GeneticVariation BEFREE We did not detect a significant difference in mortality between V122I TTR allele carriers and noncarriers, a finding that contrasts with prior observations; however, the risk of heart failure was increased among carriers. 25551524 2015
Heart failure
CUI: C0018801
Disease: Heart failure
0.060 GeneticVariation BEFREE Transthyretin amyloidosis associated with variant V122I (ATTR V122I) is likely to be an important cause of heart failure in Afro-Caribbean populations, but the high prevalence of left ventricular hypertrophy (LVH) and lack of awareness of this genetic disorder pose diagnostic hurdles. 22795285 2012
Heart failure
CUI: C0018801
Disease: Heart failure
0.060 GeneticVariation BEFREE It appears to be far less common than the previously described Val122Ile mutation but onset may be at an earlier age, potentially making heart transplantation a viable option should heart failure become severe. 23126592 2012