ClinVar Miner

List of variants in gene combination IRF8, MIR6774 reported as likely benign 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)
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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_002163.4(IRF8):c.602-6C>A	rs200999470	0.00005
NM_002163.4(IRF8):c.602-11C>T
NM_002163.4(IRF8):c.602-20C>T

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