List of variants reported as uncertain significance for parathyroid gland disorder by Genetics and Molecular Pathology, SA Pathology

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Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_001370259.2(MEN1):c.1354C>T (p.Arg452Trp)	rs863224810	0.00001
NM_000388.4(CASR):c.2054G>A (p.Gly685Asp)
NM_000388.4(CASR):c.2096C>T (p.Thr699Ile)	rs2107649929
NM_004752.4(GCM2):c.1398G>C (p.Glu466Asp)	rs537546612
NM_024529.5(CDC73):c.69C>G (p.Asp23Glu)	rs1675465120

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