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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
KIF22
(P148L +1 more)
Single nucleotide variant
(missense variant)
not provided
+2 more
GPathogenic/Likely pathogenic
ALDOA, ASPHD1
+25 more
Copy number gain
Delayed speech and language development
+8 more
GLikely pathogenic
PPP4C, PRRT2
+24 more
Copy number loss
Obesity
+2 more
GPathogenic
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