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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CLCN5
(R293C +2 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
CLCN5
Single nucleotide variant
(synonymous variant)
not provided
GUncertain significance
CLCN5
Single nucleotide variant
(synonymous variant)
not specified
+5 more
GBenign/Likely benign
CLCN5, LOC126863258
(R704Q +2 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
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