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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SLC12A6
(S471T +4 more)
Single nucleotide variant
(missense variant)
Agenesis of the corpus callosum with peripheral neuropathy
+2 more
GBenign/Likely benign
SLC12A6
Single nucleotide variant
(synonymous variant)
Inborn genetic diseases
+2 more
GBenign/Likely benign