ClinVar Miner

List of variants in gene FBXO11 reported as benign for FBXO11-related 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)
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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_001190274.2(FBXO11):c.1578A>G (p.Ala526=)	rs35935360	0.01480
NM_001190274.2(FBXO11):c.376A>T (p.Thr126Ser)	rs17036993

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