List of variants in gene combination ALAS2, LOC108663984 reported as 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_000032.5(ALAS2):c.282A>G (p.Glu94=)	rs150313977	0.00815
NM_000032.5(ALAS2):c.231C>A (p.Leu77=)	rs760900782

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