List of variants in gene IRF8 reported as benign for infectious disease

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 15

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HGVS	dbSNP	gnomAD frequency
NM_002163.4(IRF8):c.*354C>T	rs10514611	0.22551
NM_002163.4(IRF8):c.432C>T (p.Asp144=)	rs16939945	0.02710
NM_002163.4(IRF8):c.672C>T (p.Pro224=)	rs57770209	0.01766
NM_002163.4(IRF8):c.387C>T (p.Cys129=)	rs16939941	0.01293
NM_002163.4(IRF8):c.1275C>T (p.Thr425=)	rs147057451	0.01269
NM_002163.4(IRF8):c.1236A>G (p.Ser412=)	rs16940012	0.01183
NM_002163.4(IRF8):c.1194G>A (p.Pro398=)	rs2270503	0.00650
NM_002163.4(IRF8):c.894C>T (p.Phe298=)	rs61995933	0.00547
NM_002163.4(IRF8):c.813C>T (p.Phe271=)	rs147080359	0.00373
NM_002163.4(IRF8):c.864C>T (p.Phe288=)	rs372510203	0.00031
NM_002163.4(IRF8):c.1122C>T (p.Val374=)	rs544583597	0.00009
NM_002163.4(IRF8):c.1104+40del	rs10604224
NM_002163.4(IRF8):c.414C>T (p.Cys138=)	rs8052064
NM_002163.4(IRF8):c.495G>T (p.Pro165=)	rs532341216
NM_002163.4(IRF8):c.573G>A (p.Gly191=)	rs17444416

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