List of variants in gene FGFR2 reported as likely pathogenic by GeneDx

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 9

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HGVS	dbSNP	gnomAD frequency
NM_000141.5(FGFR2):c.1141T>C (p.Tyr381His)	rs387906678
NM_000141.5(FGFR2):c.1142A>G (p.Tyr381Cys)	rs1064796452
NM_000141.5(FGFR2):c.1144T>C (p.Cys382Arg)	rs121913474
NM_000141.5(FGFR2):c.1757_1758delinsGA (p.Tyr586Ter)	rs1554914180
NM_000141.5(FGFR2):c.1925T>A (p.Ile642Lys)	rs1064796413
NM_000141.5(FGFR2):c.514_515delinsTT (p.Ala172Phe)
NM_000141.5(FGFR2):c.826T>G (p.Phe276Val)	rs1057519036
NM_000141.5(FGFR2):c.842A>G (p.Tyr281Cys)	rs1057519038
NM_000141.5(FGFR2):c.958A>G (p.Thr320Ala)	rs2134260022

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