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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ARID1B, LOC115308161
(F113L +2 more)
Single nucleotide variant
(non-coding transcript variant +1 more)
Coffin-Siris syndrome 1
GUncertain significance
ARID1B
(S1386G +6 more)
Single nucleotide variant
(missense variant)
Coffin-Siris syndrome 1
GUncertain significance