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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
DLG4
(V632fs +5 more)
Indel
(frameshift variant +1 more)
Intellectual developmental disorder 62
GPathogenic
DLG4
(Y473C +5 more)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
DLG4, LOC126862479
(E244fs +5 more)
Deletion
(frameshift variant +1 more)
Intellectual developmental disorder 62
Gnot provided
DLG4
Deletion
(intron variant)
Intellectual developmental disorder 62
Gnot provided
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