List of variants in gene CDON reported as pathogenic

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: 5

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HGVS	dbSNP	gnomAD frequency
NM_001378964.1(CDON):c.2764G>A (p.Glu922Lys)	rs769676286	0.00001
NM_001378964.1(CDON):c.2818A>C (p.Ser940Arg)	rs369673018	0.00001
NM_001378964.1(CDON):c.2065C>G (p.Pro689Ala)	rs387906995
NM_001378964.1(CDON):c.2339T>A (p.Val780Glu)	rs387906996
NM_001378964.1(CDON):c.2368A>G (p.Thr790Ala)	rs387906997

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