List of variants reported as uncertain significance for parathyroid gland disorder 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: 2

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HGVS	dbSNP	gnomAD frequency
NM_001370259.2(MEN1):c.1409C>T (p.Pro470Leu)	rs750112288	0.00012
NM_001370259.2(MEN1):c.652C>T (p.Arg218Trp)	rs794728620

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