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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ANKRD11
(Q2248*)
Single nucleotide variant
(nonsense)
KBG syndrome
GPathogenic
ANKRD11
(R1007*)
Single nucleotide variant
(nonsense)
not provided
+3 more
GPathogenic/Likely pathogenic
ANKRD11
(E675fs)
Duplication
(frameshift variant)
Developmental disorder
+1 more
GPathogenic
ANKRD11
(E662fs)
Deletion
(frameshift variant)
KBG syndrome
GPathogenic
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