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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CHM
(N180fs +1 more)
Deletion
(frameshift variant)
Choroideremia
GLikely pathogenic
CHM
(A26del)
Deletion
(inframe_deletion +1 more)
Chorioretinal atrophy
+1 more
GLikely pathogenic