List of variants in gene DDX59 reported as likely pathogenic for bone development disease

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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_001031725.6(DDX59):c.1100T>G (p.Val367Gly)	rs587777067
NM_001031725.6(DDX59):c.1597-6T>G	rs546799731
NM_001031725.6(DDX59):c.1648AAT[2] (p.Asn552del)	rs1571603072

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