List of variants in gene FMN2 reported as pathogenic for carbohydrate metabolism disease

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: 5

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HGVS	dbSNP	gnomAD frequency
NM_020066.5(FMN2):c.1394dup (p.Ala466fs)	rs727502860
NM_020066.5(FMN2):c.1550del (p.Pro517fs)	rs1390970926
NM_020066.5(FMN2):c.1618C>T (p.Arg540Ter)	rs1247510585
NM_020066.5(FMN2):c.2233C>T (p.Gln745Ter)
NM_020066.5(FMN2):c.2515del (p.Thr839fs)	rs727502861

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