List of variants in gene FGF10 reported as pathogenic for bone disorder

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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: 8

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HGVS	dbSNP	gnomAD frequency
NC_000005.9:g.44300489_44312646del
NM_004465.2(FGF10):c.190G>T (p.Gly64Ter)	rs1446723373
NM_004465.2(FGF10):c.234dup (p.Trp79fs)
NM_004465.2(FGF10):c.237G>A (p.Trp79Ter)
NM_004465.2(FGF10):c.240A>C (p.Arg80Ser)	rs104893888
NM_004465.2(FGF10):c.317G>T (p.Cys106Phe)	rs104893885
NM_004465.2(FGF10):c.409A>T (p.Lys137Ter)	rs104893887
NM_004465.2(FGF10):c.467T>G (p.Ile156Arg)	rs104893886

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