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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CLCN5
(K111fs +2 more)
Deletion
(frameshift variant)
Dent disease type 1
GLikely pathogenic
CLCN5
(V251I +2 more)
Single nucleotide variant
(missense variant)
Dent disease type 1
GUncertain significance
CLCN5, LOC126863258
(C711S +2 more)
Single nucleotide variant
(missense variant)
Dent disease type 1
+3 more
GUncertain significance
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