List of variants in gene combination CUBN, LOC126860871 reported as uncertain significance 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: 5

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HGVS	dbSNP	gnomAD frequency
NM_001081.4(CUBN):c.671G>A (p.Arg224His)	rs139891639	0.00041
NM_001081.4(CUBN):c.614C>T (p.Thr205Met)	rs374652141	0.00009
NM_001081.4(CUBN):c.704G>C (p.Arg235Pro)	rs752992672	0.00001
NM_001081.4(CUBN):c.622C>T (p.Pro208Ser)
NM_001081.4(CUBN):c.685A>G (p.Ile229Val)

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