List of variants reported as uncertain significance for Noonan syndrome by Juno Genomics, Hangzhou Juno Genomics, Inc

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_006767.4(LZTR1):c.2098A>G (p.Met700Val)	rs755871821	0.00001
NM_001085049.3(MRAS):c.251C>T (p.Thr84Met)
NM_006767.4(LZTR1):c.1279_1284dup (p.Thr428_Leu429insCysThr)
NM_006767.4(LZTR1):c.2325G>A (p.Gln775=)	rs377557832

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