FKBP10, FKBP prolyl isomerase 10, 60681

N. diseases: 86; N. variants: 14
Disease: OSTEOGENESIS IMPERFECTA, TYPE XII ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs137853883
rs137853883
Entrez Id: 60681
Gene Symbol: FKBP10
FKBP10
CUI: C3151433
Disease:
OSTEOGENESIS IMPERFECTA, TYPE XII 		TC 0.700 CausalMutation CLINVAR