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Links from Gene

Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CNTN1
Deletion
Compton-North congenital myopathy
GPathogenic
CNTN1
(A788V +1 more)
Single nucleotide variant
(missense variant)
Compton-North congenital myopathy
GUncertain significance
CNTN1
Copy number gain
not provided
GUncertain significance
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