List of variants in gene HSCB reported as pathogenic 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_172002.5(HSCB):c.259dup (p.Thr87fs)	rs773607816	0.00002
NC_000022.11:g.28741962G>A	rs551244874

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