ClinVar Miner

List of variants in gene ZCCHC14 reported as likely benign for not provided

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)
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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_015144.3(ZCCHC14):c.2910C>T (p.Ser970=)	rs138128554	0.00031
NM_015144.3(ZCCHC14):c.1572C>T (p.Pro524=)	rs770768449	0.00003

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