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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SRRM2
(P1272del)
Deletion
(inframe_deletion)
Intellectual developmental disorder, autosomal dominant 72
GUncertain significance
SRRM2
Microsatellite
(inframe_insertion)
Intellectual developmental disorder, autosomal dominant 72
GUncertain significance