List of variants in gene SEMA4A reported as uncertain significance by Eurofins NTD LLC (GA)

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: 11

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HGVS	dbSNP	gnomAD frequency
NM_022367.4(SEMA4A):c.1451G>C (p.Gly484Ala)	rs148744804	0.00062
NM_022367.4(SEMA4A):c.1301T>C (p.Met434Thr)	rs146822426	0.00044
NM_022367.4(SEMA4A):c.84G>A (p.Thr28=)	rs149711133	0.00038
NM_022367.4(SEMA4A):c.1086A>C (p.Ser362=)	rs145993678	0.00024
NM_022367.4(SEMA4A):c.1123C>T (p.Arg375Trp)	rs201094714	0.00004
NM_022367.4(SEMA4A):c.1174A>C (p.Met392Leu)	rs1475557484	0.00001
NM_022367.4(SEMA4A):c.524A>G (p.Gln175Arg)	rs886042738	0.00001
NM_022367.4(SEMA4A):c.1196A>T (p.Asp399Val)	rs727504147
NM_022367.4(SEMA4A):c.1744C>T (p.His582Tyr)	rs543276469
NM_022367.4(SEMA4A):c.364-1G>T	rs794727733
NM_022367.4(SEMA4A):c.735C>A (p.Phe245Leu)	rs1553269430

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