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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC130007728, ARID2
Single nucleotide variant
(synonymous variant)
not provided
+1 more
GBenign/Likely benign
ARID2
Single nucleotide variant
(synonymous variant)
Coffin-Siris syndrome 6
+1 more
GBenign/Likely benign
ARID2
(A603V)
Single nucleotide variant
(missense variant)
Coffin-Siris syndrome 6
+1 more
GLikely benign
ARID2
(A1434S)
Single nucleotide variant
(missense variant)
Coffin-Siris syndrome 6
+1 more
GBenign
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