List of variants reported as uncertain significance for bone remodeling disease by Myriad Genetics, Inc.

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: 1

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HGVS	dbSNP	gnomAD frequency
NM_006019.4(TCIRG1):c.117+4A>C	rs751881962

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