List of variants reported as likely pathogenic for Noonan syndrome by Rady Children's Institute for Genomic Medicine, Rady Children's Hospital San Diego

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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_006767.4(LZTR1):c.510-2A>G	rs1458682620	0.00001
NM_002880.4(RAF1):c.1193G>T (p.Arg398Leu)	rs730880382

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