List of variants in gene FSCN2 reported as likely pathogenic for retinal disorder

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_001077182.3(FSCN2):c.827-1delG
NM_012418.4(FSCN2):c.1415G>C (p.Gly472Ala)
NM_012418.4(FSCN2):c.22C>T (p.Gln8Ter)

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