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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CLCN4
(Q298R +1 more)
Single nucleotide variant
(missense variant)
not provided
+1 more
GBenign/Likely benign
CLCN4
Single nucleotide variant
(synonymous variant)
not specified
+2 more
GBenign/Likely benign
CLCN4
(I574T +1 more)
Single nucleotide variant
(missense variant)
Intellectual disability, X-linked 49
+1 more
GUncertain significance
CLCN4
(T677M +1 more)
Single nucleotide variant
(missense variant)
Intellectual disability, X-linked 49
+1 more
GBenign/Likely benign
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