List of variants in gene FGFR3 reported as likely pathogenic for immune system cancer

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_000142.5(FGFR3):c.1118A>G (p.Tyr373Cys)	rs121913485
NM_000142.5(FGFR3):c.1657G>A (p.Val553Met)	rs199544087
NM_000142.5(FGFR3):c.742C>T (p.Arg248Cys)	rs121913482

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