ClinVar Miner

List of variants in gene CUBN reported as uncertain significance by Athena Diagnostics

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: 2

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HGVS	dbSNP	gnomAD frequency
NM_001081.4(CUBN):c.9079G>A (p.Gly3027Arg)	rs150202444	0.00021
NM_001081.4(CUBN):c.3496G>A (p.Gly1166Arg)	rs201443885	0.00004

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