List of variants in gene FGFR2 reported as likely pathogenic for Carcinoma of esophagus

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_000141.5(FGFR2):c.1141T>C (p.Tyr381His)	rs387906678
NM_000141.5(FGFR2):c.1144T>C (p.Cys382Arg)	rs121913474
NM_000141.5(FGFR2):c.1145G>A (p.Cys382Tyr)	rs1057519900

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