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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
KCNA1
Single nucleotide variant
(synonymous variant)
not provided
+2 more
GBenign
KCNA1
Single nucleotide variant
(synonymous variant)
Hereditary episodic ataxia
+2 more
GBenign
KCNA1
Single nucleotide variant
(synonymous variant)
KCNA1-related condition
+4 more
GBenign/Likely benign
KCNA1
Single nucleotide variant
(synonymous variant)
not provided
+3 more
GBenign
KCNA1
Single nucleotide variant
(3 prime UTR variant)
not provided
+3 more
GBenign
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