List of variants in gene DDX59 reported as uncertain significance for dysostosis

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_001031725.6(DDX59):c.27C>G (p.Ile9Met)	rs766385057	0.00001
NM_001031725.6(DDX59):c.1600G>A (p.Gly534Arg)	rs886037652
NM_001031725.6(DDX59):c.751T>C (p.Ser251Pro)	rs1571655262

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