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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
GPHN, RDH12
+1 more
Deletion
Retinal dystrophy
GLikely pathogenic
GPHN, RDH12
+1 more
(A269fs)
Deletion
(frameshift variant)
RDH12-Related Disorders
+3 more
GPathogenic