List of variants reported as likely benign for Acrocephalosyndactyly type I; Beare-Stevenson cutis gyrata syndrome; Jackson-Weiss syndrome; Pfeiffer syndrome; Antley-Bixler syndrome without genital anomalies or disordered steroidogenesis; Crouzon syndrome; Saethre-Chotzen syndrome; Familial scaphocephaly syndrome, McGillivray type; Bent bone dysplasia syndrome 1; Gastric cancer; LADD syndrome 1

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Total variants: 7

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HGVS	dbSNP	gnomAD frequency
NM_000141.5(FGFR2):c.1774C>T (p.Arg592Cys)	rs141929882	0.00012
NM_000141.5(FGFR2):c.989G>A (p.Arg330Gln)	rs199757302	0.00011
NM_000141.5(FGFR2):c.182G>A (p.Arg61His)	rs199575491	0.00007
NM_000141.5(FGFR2):c.287G>T (p.Gly96Val)	rs1277734487	0.00005
NM_000141.5(FGFR2):c.1818C>T (p.Cys606=)	rs371395564	0.00003
NM_000141.5(FGFR2):c.1348C>T (p.Arg450Cys)	rs536181987	0.00002
NM_000141.5(FGFR2):c.943G>A (p.Ala315Thr)

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