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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ADAM9
(E193fs)
Deletion
(frameshift variant +1 more)
Cone-rod dystrophy 9
GLikely pathogenic
ADAM9
Single nucleotide variant
(intron variant)
not provided
+1 more
GUncertain significance