List of variants in gene UBE2T reported as benign for inherited aplastic anemia

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_014176.4(UBE2T):c.15A>G (p.Ser5=)	rs14451	0.47315
NM_014176.4(UBE2T):c.385-11T>C	rs17490864	0.08092

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