List of variants in gene ZNF292 reported as likely pathogenic for Inborn genetic diseases

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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_015021.3(ZNF292):c.5515_5569del (p.Glu1839fs)	rs1775415071
NM_015021.3(ZNF292):c.6113_6114del (p.Val2038fs)	rs2482352325
NM_015021.3(ZNF292):c.6661_6664del (p.Leu2221fs)	rs1775494843

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