List of variants in gene FGFR2 reported as pathogenic for Inborn genetic diseases

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_000141.5(FGFR2):c.1061C>G (p.Ser354Cys)	rs121918490
NM_000141.5(FGFR2):c.1141T>G (p.Tyr381Asp)	rs387906678
NM_000141.5(FGFR2):c.314A>G (p.Tyr105Cys)	rs1434545235

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