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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
AHI1
(K1163N)
Single nucleotide variant
(3 prime UTR variant +1 more)
Joubert syndrome 3
GUncertain significance
AHI1
(K1052T)
Single nucleotide variant
(missense variant +1 more)
Joubert syndrome 3
GUncertain significance