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Links from Gene

Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SYT2
Duplication
not provided
GUncertain significance
SYT2
(L183fs)
Indel
(frameshift variant)
Congenital myasthenic syndrome 7
GLikely pathogenic
SYT2
Duplication
not provided
GLikely benign
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