Variants in gene FGFR3 with conflicting interpretations "pathogenic" and "likely pathogenic"

Submission 1 (pathogenic) minimum review status:		Submission 1 (pathogenic) method:
Submission 2 (likely pathogenic) minimum review status:		Submission 2 (likely pathogenic) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 12

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HGVS	dbSNP	gnomAD frequency
NM_000142.5(FGFR3):c.1612A>G (p.Ile538Val)	rs80053154	0.00001
NM_000142.5(FGFR3):c.1052C>G (p.Ser351Cys)	rs1057517964
NM_000142.5(FGFR3):c.1118A>G (p.Tyr373Cys)	rs121913485
NM_000142.5(FGFR3):c.1619A>C (p.Asn540Thr)	rs77722678
NM_000142.5(FGFR3):c.1620C>G (p.Asn540Lys)	rs28933068
NM_000142.5(FGFR3):c.1950G>C (p.Lys650Asn)	rs28928868
NM_000142.5(FGFR3):c.2421A>G (p.Ter807Trp)	rs121913103
NM_000142.5(FGFR3):c.667C>T (p.Arg223Cys)	rs1721198491
NM_000142.5(FGFR3):c.742C>T (p.Arg248Cys)	rs121913482
NM_000142.5(FGFR3):c.746C>G (p.Ser249Cys)	rs121913483
NM_000142.5(FGFR3):c.749C>G (p.Pro250Arg)	rs4647924
NM_000142.5(FGFR3):c.835A>T (p.Ser279Cys)	rs121913114

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