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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
NDN
(T158fs)
Duplication
(frameshift variant)
Prader-Willi syndrome
GUncertain significance
NDN
(Q71R)
Single nucleotide variant
(missense variant)
Prader-Willi syndrome
GUncertain significance
NPAP1, OCA2
+22 more
Copy number gain
Autism
+7 more
GPathogenic
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