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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
TCTN2
(P87S)
Single nucleotide variant
(missense variant)
Familial aplasia of the vermis
+4 more
GUncertain significance
TCTN2
(T223M +1 more)
Single nucleotide variant
(missense variant)
Meckel-Gruber syndrome
+6 more
GUncertain significance
TCTN2
(R330* +1 more)
Single nucleotide variant
(nonsense)
Familial aplasia of the vermis
+3 more
GPathogenic/Likely pathogenic
TCTN2
(A526T +1 more)
Single nucleotide variant
(missense variant)
Joubert syndrome 24
+3 more
GUncertain significance
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