List of variants in gene ZCCHC14 reported as benign by Breakthrough Genomics, Breakthrough Genomics

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_015144.3(ZCCHC14):c.3144C>T (p.Cys1048=)	rs73238669	0.01627
NM_015144.3(ZCCHC14):c.883C>A (p.Pro295Thr)	rs76988513	0.00429
NM_015144.3(ZCCHC14):c.1166C>T (p.Pro389Leu)	rs77379365	0.00162
NM_015144.3(ZCCHC14):c.2655C>A (p.Gly885=)	rs139009476	0.00102

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