List of variants reported as uncertain significance for parathyroid gland disorder by MGZ Medical Genetics Center

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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_000388.4(CASR):c.2671C>T (p.Arg891Cys)	rs1360294910
NM_001370259.2(MEN1):c.1388A>C (p.Glu463Ala)
NM_001370259.2(MEN1):c.758C>T (p.Ser253Leu)	rs386134259

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