List of variants in gene combination EPAS1, LOC129933654 reported as uncertain significance for bone marrow 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: 1

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HGVS	dbSNP	gnomAD frequency
NM_001430.5(EPAS1):c.-472G>A	rs886056075

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