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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ARID1B
(R35fs +3 more)
Deletion
(frameshift variant)
Coffin-Siris syndrome 1
+1 more
GPathogenic/Likely pathogenic
ARID1B
(L1083fs +2 more)
Deletion
(frameshift variant)
Coffin-Siris syndrome 1
GPathogenic
ARID1B
(S1333fs +3 more)
Duplication
(frameshift variant)
Coffin-Siris syndrome 1
GPathogenic
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