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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
NFIX
(T338M +6 more)
Single nucleotide variant
(missense variant)
Malan overgrowth syndrome
GUncertain significance
NFIX
Duplication
(inframe_insertion +1 more)
Marshall-Smith syndrome
GUncertain significance