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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
AIPL1
(W278* +6 more)
Single nucleotide variant
(nonsense +1 more)
Leber congenital amaurosis 4
+6 more
GPathogenic
AIPL1
(G129V +6 more)
Single nucleotide variant
(missense variant)
Leber congenital amaurosis 4
GUncertain significance
AIPL1
(Q155H +4 more)
Single nucleotide variant
(missense variant +1 more)
Leber congenital amaurosis 4
GPathogenic/Likely pathogenic
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