List of variants in gene CUBN reported as 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: 6

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HGVS	dbSNP	gnomAD frequency
NM_001081.4(CUBN):c.5856A>G (p.Ser1952=)	rs1801234	0.50538
NM_001081.4(CUBN):c.2487G>A (p.Ser829=)	rs1801225	0.34517
NM_001081.4(CUBN):c.9491C>G (p.Ser3164Trp)	rs57163243	0.00641
NM_001081.4(CUBN):c.3292G>T (p.Ala1098Ser)	rs146593010	0.00386
NM_001081.4(CUBN):c.1003G>A (p.Ala335Thr)	rs57335729	0.00382
NM_001081.4(CUBN):c.10383C>T (p.Ser3461=)	rs141937843	0.00363

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