List of variants in gene SEMA4A reported as likely benign for SEMA4A-related disorder

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 6

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HGVS	dbSNP	gnomAD frequency
NM_022367.4(SEMA4A):c.2249A>T (p.Asp750Val)	rs141707567	0.00137
NM_022367.4(SEMA4A):c.1047C>T (p.Val349=)	rs202047148	0.00021
NM_022367.4(SEMA4A):c.1653C>A (p.Pro551=)	rs757466000	0.00006
NM_022367.4(SEMA4A):c.822C>T (p.Gly274=)	rs761522614	0.00004
NM_022367.4(SEMA4A):c.81G>A (p.Pro27=)	rs777184442	0.00002
NM_022367.4(SEMA4A):c.996G>A (p.Gly332=)	rs377121800	0.00001

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