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Links from Gene

Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
GNB2, LOC129998974
Deletion
(splice acceptor variant)
not provided
GUncertain significance
GNB2
(L95P)
Single nucleotide variant
(missense variant)
Neurodevelopmental disorder with hypotonia and dysmorphic facies
GLikely pathogenic
GNB2
(L336V)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
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