ClinVar Miner

List of variants reported as uncertain significance for Bruck syndrome 1 by Baylor Genetics

Included ClinVar conditions (2):

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
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.1667G>A (p.Arg556His)	rs138281924	0.00120
NM_021939.4(FKBP10):c.520G>A (p.Gly174Ser)	rs140950528	0.00008
NM_021939.4(FKBP10):c.1256+8C>G	rs1206061120

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