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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
TMEM237
(Q348fs +1 more)
Duplication
(frameshift variant)
Joubert syndrome 14
GConflicting classifications of pathogenicity
TMEM237
(R18* +1 more)
Single nucleotide variant
(nonsense)
Joubert syndrome and related disorders
+1 more
GPathogenic