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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
MED13L
(D697fs)
Insertion
(frameshift variant)
MED13L-related neurodevelopmental disorder
GPathogenic
MED13L
(Q506*)
Single nucleotide variant
(nonsense)
MED13L-related neurodevelopmental disorder
GPathogenic
MED13L
(E332G)
Single nucleotide variant
(missense variant)
MED13L-related neurodevelopmental disorder
GLikely pathogenic
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