List of variants in gene EPX reported as affects 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: 3

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HGVS	dbSNP	gnomAD frequency
NM_000502.6(EPX):c.857G>A (p.Arg286His)	rs121434566	0.00009
NM_000502.6(EPX):c.1942G>A (p.Asp648Asn)	rs141055426	0.00006
NC_000017.11:g.58200228dup	rs397518446

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