Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs869025223
rs869025223
FKBP10
G 0.700 CausalMutation CLINVAR Novel FKBP10 Mutation in a Patient with Osteogenesis Imperfecta Type XI. 27362741

2016