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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
TMEM231
(L118V +1 more)
Single nucleotide variant
(missense variant +1 more)
Ciliopathy
GPathogenic
TMEM231
(L134F +1 more)
Single nucleotide variant
(missense variant +1 more)
Joubert syndrome 20
+2 more
GConflicting classifications of pathogenicity