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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
AHI1
(R610P)
Single nucleotide variant
(missense variant)
not specified
+3 more
GUncertain significance
INPP5E
(Y587H +1 more)
Single nucleotide variant
(missense variant)
Joubert syndrome 1
GLikely pathogenic
INPP5E
(A76fs)
Duplication
(frameshift variant)
Joubert syndrome 1
GPathogenic
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