Gene: FKBP10 ×
Source: UNIPROT ×
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs387906960
rs387906960
FKBP10
0.800 GeneticVariation UNIPROT Mutations in FKBP10, which result in Bruck syndrome and recessive forms of osteogenesis imperfecta, inhibit the hydroxylation of telopeptide lysines in bone collagen. 22949511

2013
dbSNP: rs397514674
rs397514674
FKBP10
0.800 GeneticVariation UNIPROT Mutations in FKBP10, which result in Bruck syndrome and recessive forms of osteogenesis imperfecta, inhibit the hydroxylation of telopeptide lysines in bone collagen. 22949511

2013
dbSNP: rs387906960
rs387906960
FKBP10
0.800 GeneticVariation UNIPROT Mutations in FKBP10 cause recessive osteogenesis imperfecta and Bruck syndrome. 20839288

2011
dbSNP: rs397514674
rs397514674
FKBP10
0.800 GeneticVariation UNIPROT Mutations in FKBP10 cause recessive osteogenesis imperfecta and Bruck syndrome. 20839288

2011
dbSNP: rs782653042
rs782653042
FKBP10
0.700 GeneticVariation UNIPROT Mutations in FKBP10, which result in Bruck syndrome and recessive forms of osteogenesis imperfecta, inhibit the hydroxylation of telopeptide lysines in bone collagen. 22949511

2013
dbSNP: rs782653042
rs782653042
FKBP10
0.700 GeneticVariation UNIPROT Mutations in FKBP10 cause recessive osteogenesis imperfecta and Bruck syndrome. 20839288

2011