ClinVar Miner

List of variants in gene IRF8, MIR6774 studied 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
		ClinVar version:

Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_002163.4(IRF8):c.602-19G>A	rs185056029	0.00107
NM_002163.4(IRF8):c.602-6C>A	rs200999470	0.00005
NM_002163.4(IRF8):c.602-11C>T
NM_002163.4(IRF8):c.602-13C>G
NM_002163.4(IRF8):c.602-20C>T

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