RS587776860 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
Autosomal dominant mendelian susceptibility to mycobacterial diseases due to partial IFNgammaR1 deficiency
Other Variants in IFNGR1