List of variants in gene USB1 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: 2

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HGVS	dbSNP	gnomAD frequency
NM_024598.4(USB1):c.387G>C (p.Leu129=)	rs542658449	0.00010
NM_024598.4(USB1):c.111C>T (p.Pro37=)	rs767672950	0.00002

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