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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
RLIM
Deletion
(inframe_deletion)
Intellectual disability, X-linked 61
GUncertain significance
RLIM
(S276P)
Single nucleotide variant
(missense variant)
Intellectual disability, X-linked 61
GUncertain significance
RLIM
(E169D)
Single nucleotide variant
(missense variant)
Intellectual disability, X-linked 61
GUncertain significance
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