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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ZBTB11
(S448R)
Single nucleotide variant
(missense variant)
Intellectual developmental disorder, autosomal recessive 69
GUncertain significance
ZBTB11
(L267F)
Single nucleotide variant
(missense variant)
Intellectual developmental disorder, autosomal recessive 69
GUncertain significance
ZBTB11
(E237K)
Single nucleotide variant
(missense variant)
Intellectual developmental disorder, autosomal recessive 69
GUncertain significance
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