List of variants in gene FBXO11 reported as likely pathogenic by Labcorp Genetics (formerly Invitae), Labcorp

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_001190274.2(FBXO11):c.1153+2T>C	rs770336997	0.00002
NM_001190274.2(FBXO11):c.1769_1778delinsGTGATGGCCC (p.His590_Gln593delinsArgAspGlyPro)	rs2104716125
NM_001190274.2(FBXO11):c.2007-1G>A	rs2104664101
NM_001190274.2(FBXO11):c.2121T>A (p.Asn707Lys)	rs2104658474

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