List of variants in gene FGFR2 reported by Mendelics

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 7

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HGVS	dbSNP	gnomAD frequency
NM_000141.5(FGFR2):c.1288-35A>G	rs41295587	0.00467
NM_000141.5(FGFR2):c.755C>T (p.Ser252Leu)	rs79184941	0.00001
NM_000141.5(FGFR2):c.1007A>G (p.Asp336Gly)	rs1057519042
NM_000141.5(FGFR2):c.1032G>A (p.Ala344=)	rs121918491
NM_000141.5(FGFR2):c.1061C>T (p.Ser354Phe)	rs121918490
NM_000141.5(FGFR2):c.1847A>G (p.Tyr616Cys)	rs762545440
NM_000141.5(FGFR2):c.940-2A>C	rs1057519041

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