ClinVar Miner

List of variants reported as likely pathogenic for Noonan syndrome 2 by Neuberg Centre For Genomic Medicine, NCGM

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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_006767.4(LZTR1):c.2428C>T (p.Arg810Trp)	rs776893978	0.00009
NM_006767.4(LZTR1):c.1397G>A (p.Arg466Gln)	rs587777180	0.00005

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