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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
AIPL1
(D286V +6 more)
Single nucleotide variant
(missense variant +1 more)
Leber congenital amaurosis 4
GUncertain significance
AIPL1
Single nucleotide variant
(intron variant)
Leber congenital amaurosis 4
GUncertain significance
AIPL1
(R80W +3 more)
Single nucleotide variant
(missense variant +1 more)
Leber congenital amaurosis 4
+1 more
GPathogenic/Likely pathogenic
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