List of variants in gene FGFR3 reported as uncertain significance for multiple congenital anomalies/dysmorphic syndrome

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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: 16

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HGVS	dbSNP	gnomAD frequency
NM_000142.5(FGFR3):c.2153A>G (p.Asn718Ser)	rs139773438	0.00011
NM_000142.5(FGFR3):c.1718C>T (p.Pro573Leu)	rs745848425	0.00003
NM_000142.5(FGFR3):c.1267G>C (p.Val423Leu)	rs1256546303	0.00002
NM_000142.5(FGFR3):c.1537G>A (p.Asp513Asn)	rs121913112	0.00002
NM_000142.5(FGFR3):c.1993G>T (p.Ala665Ser)	rs764892330	0.00002
NM_000142.5(FGFR3):c.2294C>T (p.Ala765Val)	rs140211846	0.00002
NM_000142.5(FGFR3):c.1255C>T (p.Leu419Phe)	rs770029887	0.00001
NM_000142.5(FGFR3):c.1547A>G (p.Asp516Gly)	rs772276122	0.00001
NM_000142.5(FGFR3):c.184C>T (p.Pro62Ser)	rs533866031	0.00001
NM_000142.5(FGFR3):c.200G>A (p.Gly67Asp)	rs369232922	0.00001
NM_000142.5(FGFR3):c.2413C>T (p.Arg805Trp)	rs369758941	0.00001
NM_000142.5(FGFR3):c.1537G>T (p.Asp513Tyr)
NM_000142.5(FGFR3):c.1946A>G (p.Lys649Arg)	rs1448029825
NM_000142.5(FGFR3):c.2005C>G (p.Arg669Gly)	rs1490564667
NM_000142.5(FGFR3):c.598C>T (p.Arg200Cys)	rs886043613
NM_000142.5(FGFR3):c.847C>T (p.Pro283Ser)

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