rs1555631390, TTR

N. diseases: 4
Disease: Dysautonomia ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Dysautonomia
CUI: C0013363
Disease: Dysautonomia
0.700 CausalMutation CLINVAR Unusual duplication mutation in a surface loop of human transthyretin leads to an aggressive drug-resistant amyloid disease. 29941560 2018