List of variants in gene FYCO1 reported as likely benign for Inborn genetic diseases

Minimum submission review status:		Collection method:
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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_024513.4(FYCO1):c.2612G>A (p.Arg871Gln)	rs113517878	0.00184
NM_024513.4(FYCO1):c.2749G>A (p.Val917Met)	rs373989195	0.00014
NM_024513.4(FYCO1):c.546G>A (p.Thr182=)	rs201372127	0.00014
NM_024513.4(FYCO1):c.1340G>A (p.Arg447His)	rs760218585	0.00003
NM_024513.4(FYCO1):c.1060A>G (p.Thr354Ala)
NM_024513.4(FYCO1):c.1163G>A (p.Arg388Gln)
NM_024513.4(FYCO1):c.1889G>A (p.Gly630Glu)
NM_024513.4(FYCO1):c.550A>G (p.Thr184Ala)

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