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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
GNB1
(I80T)
Single nucleotide variant
(5 prime UTR variant +1 more)
Neurodevelopmental disorder
+7 more
GPathogenic/Likely pathogenic
GNB1
(G77S)
Single nucleotide variant
(5 prime UTR variant +1 more)
Intellectual disability, autosomal dominant 42
+2 more
GPathogenic/Likely pathogenic
GNB1
(D76N)
Single nucleotide variant
(5 prime UTR variant +1 more)
Intellectual disability, autosomal dominant 42
+1 more
GPathogenic/Likely pathogenic
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