List of variants in gene IFNG reported as likely benign for anemia

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.*500C>T	rs528060683	0.00016
NM_000619.3(IFNG):c.*465A>T	rs532081510	0.00004

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