FKBP10, FKBP prolyl isomerase 10, 60681

N. diseases: 86; N. variants: 14
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs387907325
rs387907325
Entrez Id: 60681
Gene Symbol: FKBP10
FKBP10
CUI: C3151433
Disease:
OSTEOGENESIS IMPERFECTA, TYPE XII 		AT 0.700 CausalMutation CLINVAR
dbSNP: rs397509383
rs397509383
Entrez Id: 60681
Gene Symbol: FKBP10
FKBP10
CUI: C1850168
Disease:
Bruck syndrome 1 		A 0.700 CausalMutation CLINVAR
dbSNP: rs397509383
rs397509383
Entrez Id: 60681
Gene Symbol: FKBP10
FKBP10
CUI: C3151433
Disease:
OSTEOGENESIS IMPERFECTA, TYPE XII 		A 0.700 CausalMutation CLINVAR
dbSNP: rs869320752
rs869320752
Entrez Id: 60681
Gene Symbol: FKBP10
FKBP10
CUI: C1850168
Disease:
Bruck syndrome 1 		C 0.700 CausalMutation CLINVAR
dbSNP: rs13412
rs13412
Entrez Id: 10609;60681
Gene Symbol: P3H4;FKBP10
P3H4;FKBP10
CUI: C0007785
Disease:
Cerebral Infarction 		0.010 GeneticVariation BEFREE Rs19203 and rs13412 in the promoter region of the ATP2B1 gene are correlated with the onset of CI. 31173308 2019