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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
MED13
(T1496fs)
Deletion
(frameshift variant)
Intellectual developmental disorder 61
GPathogenic
MED13
(L582*)
Single nucleotide variant
(nonsense)
not provided
GPathogenic
MED13
(T326I)
Single nucleotide variant
(missense variant)
Intellectual developmental disorder 61
GPathogenic
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