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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
POGZ
(L1027P +4 more)
Single nucleotide variant
(missense variant)
Intellectual disability-microcephaly-strabismus-behavioral abnormalities syndrome
GUncertain significance
POGZ
(W1025G +4 more)
Single nucleotide variant
(missense variant)
Intellectual disability-microcephaly-strabismus-behavioral abnormalities syndrome
GUncertain significance