List of variants in gene HBG1 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: 5

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HGVS	dbSNP	gnomAD frequency
NM_000559.3(HBG1):c.410C>G (p.Ala137Gly)	rs56205611	0.00681
NM_000559.3(HBG1):c.*3T>C	rs62755960
NM_000559.3(HBG1):c.*4C>T	rs61893083
NM_000559.3(HBG1):c.*5A>C	rs1065686
NM_000559.3(HBG1):c.*6C>T	rs5009539

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