List of variants in gene combination CUBN, LOC126860871 reported as 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: 3

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HGVS	dbSNP	gnomAD frequency
NM_001081.4(CUBN):c.594-34G>A	rs2295813	0.91875
NM_001081.4(CUBN):c.618C>T (p.Tyr206=)	rs41289313	0.06126
NM_001081.4(CUBN):c.657G>A (p.Gly219=)	rs142553474	0.00566

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