List of variants in gene CCDC40 reported as benign 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: 6

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HGVS	dbSNP	gnomAD frequency
NM_017950.4(CCDC40):c.207G>C (p.Val69=)	rs2289527	0.98631
NM_017950.4(CCDC40):c.630C>T (p.Ser210=)	rs117419007	0.00481
NM_017950.4(CCDC40):c.3424T>C (p.Ser1142Pro)	rs148900528	0.00366
NM_017950.4(CCDC40):c.3349G>A (p.Glu1117Lys)	rs145595957	0.00365
NM_017950.4(CCDC40):c.3408C>T (p.Leu1136=)	rs186591691	0.00309
NM_017950.4(CCDC40):c.180G>A (p.Ala60=)	rs185006459	0.00183

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