List of variants in gene combination IFNAR2, IFNAR2-IL10RB 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: 4

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HGVS	dbSNP	gnomAD frequency
NM_207585.3(IFNAR2):c.555_559del (p.Ile185fs)	rs1312285586	0.00006
NM_001289125.3(IFNAR2):c.311del (p.Glu104fs)	rs775739391	0.00001
NM_001289125.3(IFNAR2):c.157T>C (p.Ser53Pro)	rs1987287426
NM_207585.3(IFNAR2):c.236del (p.Asp78_Leu79insTer)	rs1310889473

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