ClinVar Miner

List of variants in gene FMN2 reported as likely benign by Department of Genetics, Rouen University Hospital, Normandy Center for Genomic and Personalized Medicine

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_020066.5(FMN2):c.4619C>T (p.Ser1540Leu)	rs150801382	0.00221
NM_020066.5(FMN2):c.3825G>T (p.Gly1275=)	rs901699283

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