RS35744605 IFIH1
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What This Variant Does
"CLNSIG=3
Associated Conditions
Singleton-Merten syndrome 1
Aicardi-Goutieres syndrome 7
IFIH1-related immunodeficiency
Immunodeficiency 95
Inborn genetic diseases
IFIH1-related disorder
Singleton-Merten syndrome 1
Aicardi-Goutieres syndrome 7
IFIH1-related immunodeficiency
Immunodeficiency 95
Inborn genetic diseases
IFIH1-related disorder
Other Variants in IFIH1