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Links from Gene

Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
RPL10L
(I167M)
Single nucleotide variant
(missense variant)
Intellectual developmental disorder with dysmorphic facies and ptosis
GUncertain significance
RPL10L
Copy number gain
not provided
GLikely benign
RPL10L
Copy number loss
See cases
GUncertain significance
RPL10L
(R32C)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
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