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

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Total variants: 13

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HGVS	dbSNP	gnomAD frequency
NM_006767.4(LZTR1):c.628C>T (p.Arg210Ter)	rs150419186	0.00010
NM_006767.4(LZTR1):c.1943-256C>T	rs761685529	0.00008
NM_006767.4(LZTR1):c.1396C>T (p.Arg466Trp)	rs550922200	0.00006
NM_006767.4(LZTR1):c.2387T>C (p.Ile796Thr)	rs141672122	0.00004
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.465C>G (p.Tyr155Ter)	rs753295968	0.00001
NM_006767.4(LZTR1):c.1321C>T (p.Gln441Ter)	rs2518620018
NM_006767.4(LZTR1):c.1602del (p.Lys534fs)	rs1268674934
NM_006767.4(LZTR1):c.2011_2012del (p.Leu671fs)	rs772226479
NM_006767.4(LZTR1):c.2090G>A (p.Arg697Gln)	rs370638947
NM_006767.4(LZTR1):c.27dup (p.Gln10fs)	rs587777613
NM_006767.4(LZTR1):c.955del (p.Gln319fs)	rs1386054181

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