RS587776856 IFNGR1
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What This Variant Does
"CLNSIG=5
Associated Conditions
Autosomal dominant mendelian susceptibility to mycobacterial diseases due to partial IFNgammaR1 deficiency
IFN-gamma receptor 1 deficiency
Disseminated atypical mycobacterial infection
Mycobacterium tuberculosis
susceptibility to
Helicobacter pylori infection
Hepatitis B virus
Immunodeficiency 27A
Autosomal dominant mendelian susceptibility to mycobacterial diseases due to partial IFNgammaR1 deficiency
IFN-gamma receptor 1 deficiency
Disseminated atypical mycobacterial infection
Mycobacterium tuberculosis
susceptibility to
Helicobacter pylori infection
Hepatitis B virus
Other Variants in IFNGR1