List of variants in gene SPAG1 reported as uncertain significance by GeneDx

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_003114.5(SPAG1):c.1476T>C (p.Asn492=)	rs377184852	0.00002
NM_003114.5(SPAG1):c.1063G>T (p.Gly355Ter)
NM_003114.5(SPAG1):c.1960A>G (p.Asn654Asp)	rs1818756163
NM_003114.5(SPAG1):c.2585T>C (p.Ile862Thr)	rs2489646379
NM_003114.5(SPAG1):c.655G>C (p.Ala219Pro)	rs2489325167

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