List of variants in gene ZNF83 reported as likely benign by Ambry 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: 3

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HGVS	dbSNP	gnomAD frequency
NM_018300.4(ZNF83):c.1142C>T (p.Ala381Val)
NM_018300.4(ZNF83):c.1315G>A (p.Gly439Ser)	rs778743816
NM_018300.4(ZNF83):c.1430C>T (p.Ala477Val)	rs149457093

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