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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
IFIH1
(K983E)
Single nucleotide variant
(missense variant)
Basal ganglia calcification, idiopathic, childhood-onset
+2 more
GUncertain significance
IFIH1
(R618Q)
Single nucleotide variant
(missense variant)
not provided
+3 more
GConflicting classifications of pathogenicity
IFIH1
(R77W)
Single nucleotide variant
(missense variant)
IFIH1-related condition
+4 more
GConflicting classifications of pathogenicity
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