"SEMA4A-related disorder"[Disease/phenotype] AND "PreventionGenetics, - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3051241	NM_022367.4(SEMA4A):c.81G>A (p.Pro27=)	SEMA4A	Single nucleotide variant (synonymous variant +2 more)	SEMA4A-related disorder	GLikely benign
Select item 1664634	NM_022367.4(SEMA4A):c.822C>T (p.Gly274=)	SEMA4A	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 3034117	NM_022367.4(SEMA4A):c.996G>A (p.Gly332=)	SEMA4A	Single nucleotide variant (synonymous variant)	SEMA4A-related disorder	GLikely benign
Select item 749432	NM_022367.4(SEMA4A):c.1047C>T (p.Val349=)	SEMA4A	Single nucleotide variant (synonymous variant)	SEMA4A-related disorder +1 more	GLikely benign
Select item 727396	NM_022367.4(SEMA4A):c.1653C>A (p.Pro551=)	SEMA4A	Single nucleotide variant (synonymous variant)	not provided +3 more	GConflicting classifications of pathogenicity
Select item 746667	NM_022367.4(SEMA4A):c.2249A>T (p.Asp750Val)	SEMA4A (D618V +3 more)	Single nucleotide variant (missense variant)	not provided +3 more	GConflicting classifications of pathogenicity

ClinVar