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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ASXL3
(S561*)
Single nucleotide variant
(nonsense)
Severe feeding difficulties-failure to thrive-microcephaly due to ASXL3 deficiency syndrome
GPathogenic
ASXL3
(S2214P)
Single nucleotide variant
(missense variant)
Severe feeding difficulties-failure to thrive-microcephaly due to ASXL3 deficiency syndrome
GUncertain significance
AQP4, ASXL3
+35 more
Copy number loss
See cases
GPathogenic
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