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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SLC12A6
(L633R +4 more)
Single nucleotide variant
(missense variant)
Agenesis of the corpus callosum with peripheral neuropathy
GUncertain significance
SLC12A6
(Q527fs +4 more)
Deletion
(frameshift variant)
Peripheral neuropathy
GLikely pathogenic