List of variants in gene IFNG 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_000619.3(IFNG):c.*180C>T	rs2069722	0.01606
NM_000619.3(IFNG):c.*539A>G	rs2069723	0.01255

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