GENETIC ENCYCLOPEDIA
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disease: Immunodeficiency 32b

id1248
nameImmunodeficiency 32b
variant-disease NM_002163.4(IRF8):c.602C>T (p.Ala201Val) AND Immunodeficiency 32b
NM_002163.4(IRF8):c.322A>G (p.Lys108Glu) AND Immunodeficiency 32b
NM_002163.4(IRF8):c.671C>T (p.Pro224Leu) AND Immunodeficiency 32b
NM_002163.4(IRF8):c.406A>G (p.Met136Val) AND multiple conditions
NM_002163.4(IRF8):c.1030G>A (p.Gly344Ser) AND multiple conditions
... 34 more