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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ARID1B, LOC115308161
+1 more
(A7G +1 more)
Single nucleotide variant
(missense variant)
ARID1B-related disorder
GUncertain significance
ARID1B, LOC115308161
+1 more
(A92G +1 more)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
LOC115308161, LOC129997523
+1 more
Single nucleotide variant
(synonymous variant)
ARID1B-related disorder
+4 more
GBenign/Likely benign
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