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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
TMEM216
(V47A)
Single nucleotide variant
(missense variant +1 more)
Joubert syndrome 2
+4 more
GConflicting classifications of pathogenicity
TMEM216
(F36I +1 more)
Single nucleotide variant
(missense variant)
not provided
+4 more
GUncertain significance