RS376048533 IFIH1
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What This Variant Does
"CLNSIG=5
Associated Conditions
Singleton-Merten syndrome 1
Aicardi-Goutieres syndrome 7
IFIH1-related disorder
Inborn genetic diseases
Incidental Discovery
Singleton-Merten syndrome 1
Aicardi-Goutieres syndrome 7
Singleton-Merten syndrome 1
Aicardi-Goutieres syndrome 7
IFIH1-related disorder
Inborn genetic diseases
Incidental Discovery
Singleton-Merten syndrome 1
Aicardi-Goutieres syndrome 7
Other Variants in IFIH1