List of variants in gene combination CUBN, LOC126860871 reported as likely pathogenic for nutritional disorder

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.703C>T (p.Arg235Ter)	rs1461982823	0.00001
NM_001081.4(CUBN):c.673T>A (p.Cys225Ser)	rs386833790

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