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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
STIL
(L485F +1 more)
Single nucleotide variant
(missense variant)
not provided
+3 more
GBenign/Likely benign
STIL
(S409T +1 more)
Single nucleotide variant
(missense variant)
Abnormal brain morphology
GLikely pathogenic