rs267607161, TTR

N. diseases: 16
Disease: Fabry Disease ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Fabry Disease
CUI: C0002986
Disease: Fabry Disease
0.010 GeneticVariation BEFREE Fabry disease (1%) and familial amyloid polyneuropathy (3%) with Ala97Ser transthyretin (TTR) mutations were also detected. 28957343 2017