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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SLC12A6
(R716C +4 more)
Single nucleotide variant
(missense variant)
not provided
+2 more
GUncertain significance
SLC12A6
(A200fs +4 more)
Deletion
(frameshift variant)
not provided
+1 more
GPathogenic/Likely pathogenic
SLC12A6
(G15R)
Single nucleotide variant
(missense variant +1 more)
Agenesis of the corpus callosum with peripheral neuropathy
GUncertain significance
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