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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
TMEM138
(N25S)
Single nucleotide variant
(non-coding transcript variant +2 more)
Joubert syndrome 16
+2 more
GUncertain significance
TMEM138
Single nucleotide variant
(synonymous variant +1 more)
Joubert syndrome 16
+1 more
GBenign