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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ADAMTS18
(W1127* +1 more)
Single nucleotide variant
(nonsense)
Microcornea-myopic chorioretinal atrophy
+1 more
GPathogenic/Likely pathogenic
ADAMTS18
(R1053W +1 more)
Single nucleotide variant
(missense variant)
Retinitis pigmentosa
+3 more
GConflicting classifications of pathogenicity
ADAMTS18
(K918E +1 more)
Single nucleotide variant
(missense variant)
not provided
+3 more
GConflicting classifications of pathogenicity
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