List of variants in gene RBFOX1 reported as likely 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_018723.4(RBFOX1):c.96C>G (p.Pro32=)	rs143695164	0.00052
NM_001415887.1(RBFOX1):c.438C>T (p.Ser146=)
NM_018723.4(RBFOX1):c.51C>A (p.Ala17=)	rs139265655

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