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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ARID1B
(N72fs +2 more)
Deletion
(frameshift variant)
Coffin-Siris syndrome 1
GLikely pathogenic
ARID1B
(Q1489* +6 more)
Single nucleotide variant
(nonsense)
not provided
+1 more
GPathogenic/Likely pathogenic
ARID1B
(E1756fs +4 more)
Deletion
(frameshift variant)
Marfanoid habitus and intellectual disability
+2 more
GPathogenic/Likely pathogenic
ARID1B
(S1516L +6 more)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
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