List of variants reported as uncertain significance for parathyroid gland disorder by Institute of Human Genetics, University of Leipzig Medical Center

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Total variants: 6

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HGVS	dbSNP	gnomAD frequency
NM_001370259.2(MEN1):c.803A>G (p.Tyr268Cys)	rs773500082	0.00006
NM_001370259.2(MEN1):c.1003C>T (p.Arg335Trp)	rs371364206
NM_001370259.2(MEN1):c.1185+1G>A	rs1941661315
NM_001370259.2(MEN1):c.1780A>G (p.Thr594Ala)	rs1941488490
NM_024529.5(CDC73):c.192TAA[1] (p.Asn66del)
NM_080425.4(GNAS):c.1005G>T (p.Pro335=)	rs536976542

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