List of variants in gene CUBN reported as uncertain significance by 3billion

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_001081.4(CUBN):c.6095G>A (p.Cys2032Tyr)	rs201720797	0.00003
NM_001081.4(CUBN):c.6821+3A>G	rs767078847	0.00001
NM_001081.4(CUBN):c.4790T>C (p.Leu1597Pro)
NM_001081.4(CUBN):c.8579G>A (p.Cys2860Tyr)	rs2131416995

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