List of variants in gene ZNF292 reported as likely pathogenic by GeneDx

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: 9

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HGVS	dbSNP	gnomAD frequency
NM_015021.3(ZNF292):c.1672C>T (p.Arg558Ter)	rs373131243
NM_015021.3(ZNF292):c.1897C>T (p.Arg633Ter)	rs1775161294
NM_015021.3(ZNF292):c.2320C>G (p.His774Asp)	rs2127859619
NM_015021.3(ZNF292):c.3384del (p.Ala1129fs)	rs2127862824
NM_015021.3(ZNF292):c.4897A>T (p.Lys1633Ter)	rs1775368255
NM_015021.3(ZNF292):c.5367_5370del (p.Asn1790fs)	rs2482341145
NM_015021.3(ZNF292):c.5402_5403del (p.Val1801fs)	rs2127869216
NM_015021.3(ZNF292):c.6145dup (p.Ser2049fs)	rs764995318
NM_015021.3(ZNF292):c.7003C>T (p.Arg2335Ter)	rs1168689294

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