List of variants in gene combination HAX1, LOC129931498 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_006118.4(HAX1):c.-58T>G	rs11265425	0.21409
NM_006118.4(HAX1):c.-52G>T	rs578086387	0.00009

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