List of variants in gene IRF7 reported as pathogenic for immune system 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_001572.5(IRF7):c.1261C>T (p.Gln421Ter)	rs375323253	0.00001
NM_001572.5(IRF7):c.1228T>G (p.Phe410Val)	rs786205223

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