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Links from Gene

Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CAPRIN1
(R297fs)
Deletion
(frameshift variant)
Juvenile myoclonic epilepsy
GPathogenic
CAPRIN1
(L362F)
Single nucleotide variant
(missense variant)
Autism spectrum disorder
GLikely benign
CAPRIN1
(P683T)
Single nucleotide variant
(missense variant)
See cases
GUncertain significance
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