List of variants in gene FBXO8 reported as benign for not provided

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_012180.3(FBXO8):c.773-3C>T	rs115274413	0.00859
NM_012180.3(FBXO8):c.882C>T (p.Arg294=)	rs77119323	0.00735
NM_012180.3(FBXO8):c.368A>G (p.Asn123Ser)	rs61748174	0.00347

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