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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
KCNJ12
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
KCNJ12
(A133D)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
KCNJ12, LINC02693
+1 more
Copy number gain
not provided
GLikely benign
KCNJ12, LINC02693
Copy number gain
not provided
GUncertain significance
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