List of variants in gene CUBN reported as likely benign for not specified

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_001081.4(CUBN):c.2594G>A (p.Ser865Asn)	rs138083522	0.00719
NM_001081.4(CUBN):c.1681G>A (p.Asp561Asn)	rs147449194	0.00181
NM_001081.4(CUBN):c.8968G>A (p.Val2990Ile)	rs115888073	0.00169

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