List of variants in gene ZCCHC14 reported as likely benign

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: 7

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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.2083G>A (p.Ala695Thr)	rs141001038	0.00028
NM_015144.3(ZCCHC14):c.1210A>G (p.Ser404Gly)	rs537779885	0.00010
NM_015144.3(ZCCHC14):c.1572C>T (p.Pro524=)	rs770768449	0.00003
NM_015144.3(ZCCHC14):c.1667A>G (p.Tyr556Cys)
NM_015144.3(ZCCHC14):c.1907G>C (p.Ser636Thr)
NM_015144.3(ZCCHC14):c.2866G>A (p.Val956Met)

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