List of variants in gene FBXO11 reported as uncertain significance by Laboratorio de Genetica e Diagnostico Molecular, Hospital Israelita Albert Einstein

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: 6

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HGVS	dbSNP	gnomAD frequency
NM_001190274.2(FBXO11):c.1248A>G (p.Thr416=)	rs1308198485
NM_001190274.2(FBXO11):c.1586G>C (p.Trp529Ser)	rs2104738565
NM_001190274.2(FBXO11):c.1787G>A (p.Gly596Glu)
NM_001190274.2(FBXO11):c.1799A>G (p.His600Arg)	rs2104703613
NM_001190274.2(FBXO11):c.1981_1983del (p.His661del)
NM_001190274.2(FBXO11):c.571A>G (p.Asn191Asp)

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