List of variants in gene SEMA4A reported as uncertain significance by Blueprint 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: 3

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HGVS	dbSNP	gnomAD frequency
NM_022367.4(SEMA4A):c.302T>C (p.Ile101Thr)	rs149652495	0.00016
NM_022367.4(SEMA4A):c.224C>G (p.Thr75Ser)	rs768178231	0.00002
NM_022367.4(SEMA4A):c.2175_2176dup (p.Glu726fs)	rs780625314

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