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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SLC6A1, SLC6A1-AS1
(R44Q)
Single nucleotide variant
(missense variant +1 more)
not provided
+1 more
GPathogenic
SLC6A1
(A389V +2 more)
Single nucleotide variant
(missense variant)
Myoclonic-astatic epilepsy
GUncertain significance
SLC6A1
(V451fs +2 more)
Deletion
(frameshift variant)
Myoclonic-astatic epilepsy
GPathogenic
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