List of variants in gene ZNF462 reported as likely pathogenic 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)
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_021224.6(ZNF462):c.2977_2979delinsTGGTG (p.Pro993fs)	rs1564106503
NM_021224.6(ZNF462):c.3898C>T (p.Arg1300Ter)	rs1176008720
NM_021224.6(ZNF462):c.5999C>A (p.Ser2000Ter)

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