ClinVar Miner

List of variants in gene FBXO4 reported as likely benign

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)
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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_012176.3(FBXO4):c.522G>A (p.Gln174=)	rs144096644	0.00114
NM_012176.3(FBXO4):c.1154G>A (p.Arg385His)	rs747740555	0.00001

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