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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
KCNA4
(K608N)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
KCNA4
(R89Q)
Single nucleotide variant
(missense variant)
Microcephaly, cataracts, impaired intellectual development, and dystonia with abnormal striatum
GUncertain significance