List of variants in gene FOXI3 reported as likely pathogenic for bone disorder

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: 13

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HGVS	dbSNP	gnomAD frequency
NM_001135649.3(FOXI3):c.1243C>T (p.Arg415Ter)	rs1456659870	0.00001
NM_001135649.3(FOXI3):c.707G>A (p.Arg236Gln)	rs182321240	0.00001
NM_001135649.3(FOXI3):c.719G>A (p.Arg240His)	rs1370585001	0.00001
NM_001135649.3(FOXI3):c.1105AGCAATAGCACC[1] (p.369SNST[1])	rs767872970
NM_001135649.3(FOXI3):c.305T>A (p.Phe102Tyr)	rs2528917171
NM_001135649.3(FOXI3):c.596T>G (p.Leu199Arg)	rs2528916190
NM_001135649.3(FOXI3):c.673T>C (p.Cys225Arg)	rs2528910551
NM_001135649.3(FOXI3):c.700T>G (p.Phe234Val)	rs2528910500
NM_001135649.3(FOXI3):c.702C>A (p.Phe234Leu)	rs955268781
NM_001135649.3(FOXI3):c.703C>T (p.Arg235Cys)	rs1316696594
NM_001135649.3(FOXI3):c.706C>T (p.Arg236Trp)	rs1675993398
NM_001135649.3(FOXI3):c.713G>A (p.Arg238Gln)	rs923448937
NM_001135649.3(FOXI3):c.718C>T (p.Arg240Cys)	rs1451029499

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