List of variants reported as uncertain significance for Noonan syndrome 2

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Total variants: 14

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HGVS	dbSNP	gnomAD frequency
NM_006767.4(LZTR1):c.594-3C>T	rs373968693	0.00015
NM_006767.4(LZTR1):c.1943-256C>T	rs761685529	0.00009
NM_006767.4(LZTR1):c.1303C>T (p.Arg435Trp)	rs369722558	0.00008
NM_006767.4(LZTR1):c.1055A>C (p.Tyr352Ser)	rs368649599	0.00006
NM_006767.4(LZTR1):c.2260A>C (p.Asn754His)	rs745755957	0.00005
NM_006767.4(LZTR1):c.1403G>A (p.Arg468His)	rs146427018	0.00004
NM_006767.4(LZTR1):c.2317G>A (p.Val773Met)	rs199586863	0.00004
NM_006767.4(LZTR1):c.1385T>C (p.Ile462Thr)	rs147684991	0.00003
NM_006767.4(LZTR1):c.2246A>G (p.Tyr749Cys)	rs755260815	0.00001
NM_006767.4(LZTR1):c.2462T>C (p.Ile821Thr)	rs1275511136	0.00001
NM_006767.4(LZTR1):c.1382C>A (p.Ala461Asp)	rs1569156890
NM_006767.4(LZTR1):c.1888C>T (p.Arg630Trp)	rs750813513
NM_006767.4(LZTR1):c.2102C>T (p.Pro701Leu)
NM_006767.4(LZTR1):c.2325G>T (p.Gln775His)

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