Source: BEFREE ×
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs267607161
rs267607161
TTR
0.020 GeneticVariation BEFREE Cardiac manifestations and prognostic implications of hereditary transthyretin amyloidosis associated with transthyretin Ala97Ser. 31521469

2020
dbSNP: rs267607161
rs267607161
TTR
0.020 GeneticVariation BEFREE Herein, we demonstrate genetic confirmation of the ATTR Ala97Ser mutation, the most common endemic mutation in Taiwan. 29939164

2018