List of variants in gene combination EPAS1, LOC126806210 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_001430.5(EPAS1):c.525G>A (p.Thr175=)	rs115264325	0.00137
NM_001430.5(EPAS1):c.587C>A (p.Thr196Lys)	rs780349023

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