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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ARID1B
Single nucleotide variant
(synonymous variant)
Coffin-Siris syndrome 1
GUncertain significance
ARID1B
(T1581A +6 more)
Single nucleotide variant
(missense variant)
Coffin-Siris syndrome 1
GLikely benign
ARID1B
Single nucleotide variant
(synonymous variant)
Coffin-Siris syndrome 1
GLikely benign
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