List of variants in gene combination IRF8, LOC130059663 reported as uncertain significance for Immunodeficiency 32B; Mendelian susceptibility to mycobacterial diseases due to partial IRF8 deficiency

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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_002163.4(IRF8):c.332G>A (p.Arg111Gln)	rs371942842
NM_002163.4(IRF8):c.343G>C (p.Glu115Gln)
NM_002163.4(IRF8):c.358+4A>C
NM_002163.4(IRF8):c.358+4A>T

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