List of variants in gene HABP2 reported as likely benign for hematologic disorder

Minimum submission review status:		Collection method:
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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_004132.5(HABP2):c.364C>T (p.Arg122Trp)	rs78201625	0.00179
NM_004132.5(HABP2):c.947G>A (p.Gly316Glu)	rs138864377	0.00076

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