List of variants in gene FMN2 reported as benign for autosomal recessive disease

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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: 8

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HGVS	dbSNP	gnomAD frequency
NM_020066.5(FMN2):c.3442A>G (p.Arg1148Gly)	rs12732924	0.45161
NM_020066.5(FMN2):c.1413C>A (p.Ala471=)	rs10926124	0.38564
NM_020066.5(FMN2):c.2517C>G (p.Thr839=)	rs10926166	0.34857
NM_020066.5(FMN2):c.4403G>A (p.Arg1468His)	rs3795677	0.29272
NM_020066.5(FMN2):c.1830A>G (p.Ser610=)	rs3765588	0.22473
NM_020066.5(FMN2):c.3216G>A (p.Ala1072=)	rs71646895	0.04951
NM_020066.5(FMN2):c.162CGG[4] (p.Gly59del)	rs71929261
NM_020066.5(FMN2):c.162del (p.Gly55fs)	rs1572736047

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