List of variants in gene SEMA4F reported as likely benign by Ambry Genetics

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: 5

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HGVS	dbSNP	gnomAD frequency
NM_004263.5(SEMA4F):c.691G>A (p.Val231Met)	rs375402877	0.00012
NM_004263.5(SEMA4F):c.1817C>T (p.Ala606Val)	rs773358389	0.00002
NM_004263.5(SEMA4F):c.1175G>A (p.Arg392Gln)
NM_004263.5(SEMA4F):c.1964G>A (p.Arg655Gln)
NM_004263.5(SEMA4F):c.956T>C (p.Leu319Pro)

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