List of variants reported as likely pathogenic for endocrine gland neoplasm by Neuberg Centre For Genomic Medicine, NCGM

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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_004482.4(GALNT3):c.16C>T (p.Arg6Ter)	rs376963628	0.00029
NM_000388.4(CASR):c.493-2A>C	rs1576857818

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