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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SEMA4A
(P393L +3 more)
Single nucleotide variant
(missense variant)
Cone-rod dystrophy 10
+2 more
GUncertain significance
SEMA4A
(R723C +3 more)
Single nucleotide variant
(missense variant)
not provided
+5 more
GBenign/Likely benign
SEMA4A
(A751T +3 more)
Single nucleotide variant
(missense variant)
Cone-rod dystrophy 10
+4 more
GUncertain significance
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