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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ARID1B
(R1360S +6 more)
Single nucleotide variant
(missense variant)
Coffin-Siris syndrome 1
GUncertain significance
ARID1B
(L1425fs +3 more)
Duplication
(frameshift variant)
Coffin-Siris syndrome 1
GPathogenic