List of variants in gene combination CUBN, LOC129390143 reported as likely benign for hematologic 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: 4

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HGVS	dbSNP	gnomAD frequency
NM_001081.4(CUBN):c.1236T>C (p.Thr412=)	rs201404467	0.00012
NM_001081.4(CUBN):c.1350C>T (p.Gly450=)	rs770827241	0.00001
NM_001081.4(CUBN):c.1231-10T>C
NM_001081.4(CUBN):c.1231-9T>C

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