List of variants in gene combination IFNAR2-IL10RB, IL10RB reported as likely 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_000628.5(IL10RB):c.611G>A (p.Trp204Ter)	rs1329427406	0.00001
NM_000628.5(IL10RB):c.173+2T>G	rs2123561272
NM_000628.5(IL10RB):c.174-1G>A
NM_000628.5(IL10RB):c.331+1G>C	rs1989179205

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