List of variants in gene CCDC39 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: 3

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HGVS	dbSNP	gnomAD frequency
NM_181426.2(CCDC39):c.1035-5T>C	rs200089274	0.00024
NM_181426.2(CCDC39):c.641G>A (p.Arg214His)	rs368553676	0.00010
NM_181426.2(CCDC39):c.1034G>A (p.Arg345Lys)	rs1445203962	0.00001

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