ClinVar Miner

List of variants in gene FKBP10 reported as likely pathogenic for Bruck syndrome

Included ClinVar conditions (4):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 3
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HGVS dbSNP gnomAD frequency
NM_021939.4(FKBP10):c.344G>A (p.Arg115Gln) rs387906960 0.00001
NM_021939.4(FKBP10):c.179A>C (p.Gln60Pro) rs2144041758
NM_021939.4(FKBP10):c.890_897dup (p.Gly300Ter) rs1567855132

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