List of variants reported as uncertain significance for breast cancer by MVZ Praenatalmedizin und Genetik Nuernberg

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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_004360.5(CDH1):c.1633C>T (p.Arg545Trp)	rs863224727	0.00001
NM_024675.4(PALB2):c.2756T>G (p.Val919Gly)	rs886041103

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