List of variants in gene FKBP10 reported as likely pathogenic for Bruck syndrome 1

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		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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