Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs104894665
rs104894665
TTR
0.010 GeneticVariation BEFREE In this kindred, oculoleptomeningeal amyloidosis is related to a mutation in transthyretin (Phe64Ser). 10488818

1999