List of variants reported as uncertain significance for Noonan syndrome 10 by Victorian Clinical Genetics Services, Murdoch Childrens Research Institute

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_006767.4(LZTR1):c.2260A>C (p.Asn754His)	rs745755957	0.00005
NM_006767.4(LZTR1):c.1667G>A (p.Ser556Asn)
NM_006767.4(LZTR1):c.1685_1702dup (p.Arg567_Gln568insLeuGluGlnLeuCysArg)	rs1924752851
NM_006767.4(LZTR1):c.2325G>T (p.Gln775His)

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