List of variants in gene FSCN2 reported as benign by CeGaT Center for Human Genetics Tuebingen

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_012418.4(FSCN2):c.966C>T (p.His322=)	rs367734858	0.00848
NM_012418.4(FSCN2):c.1092C>T (p.Ile364=)	rs188142101	0.00195
NM_012418.4(FSCN2):c.829G>A (p.Val277Ile)	rs181420326

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