ClinVar Miner

List of variants in gene CCDC39 reported as likely benign by Fulgent Genetics, Fulgent 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: 2

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HGVS	dbSNP	gnomAD frequency
NM_181426.2(CCDC39):c.2159-16A>C	rs147028259	0.00812
NM_181426.2(CCDC39):c.1363-13del	rs374074877

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