PPIB, peptidylprolyl isomerase B, 5479

N. diseases: 59; N. variants: 8
Disease: OSTEOGENESIS IMPERFECTA, TYPE IX (disorder) ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs137853866
rs137853866
Entrez Id: 5479
Gene Symbol: PPIB
PPIB
CUI: C1850169
Disease:
OSTEOGENESIS IMPERFECTA, TYPE IX (disorder) 		T 0.700 CausalMutation CLINVAR