List of variants reported as likely pathogenic for Noonan syndrome 2 by Women's Health and Genetics/Laboratory Corporation of America, LabCorp

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_006767.4(LZTR1):c.1785+1G>A	rs145594158	0.00001
NM_006767.4(LZTR1):c.2407-2A>G	rs1158550690	0.00001
NM_006767.4(LZTR1):c.2090G>A (p.Arg697Gln)	rs370638947
NM_006767.4(LZTR1):c.27dup (p.Gln10fs)	rs587777613

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