List of variants in gene combination CUBN, LOC126860871 reported as likely benign 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: 7

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HGVS	dbSNP	gnomAD frequency
NM_001081.4(CUBN):c.720+12C>A	rs888514621	0.00001
NM_001081.4(CUBN):c.594-16C>T
NM_001081.4(CUBN):c.594-18C>T	rs1836875187
NM_001081.4(CUBN):c.615G>T (p.Thr205=)
NM_001081.4(CUBN):c.645C>T (p.Asp215=)
NM_001081.4(CUBN):c.720+20G>A
NM_001081.4(CUBN):c.720+8C>T

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