List of variants in gene combination IFNGR2, LOC119266102 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_005534.4(IFNGR2):c.1A>G (p.Met1Val)	rs1316638883	0.00001
NM_005534.4(IFNGR2):c.4del (p.Arg2fs)	rs2083655919

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