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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
C20orf141, CPXM1
+30 more
Copy number gain
See cases
GUncertain significance
IDH3B, LOC129391150
(N386S +1 more)
Single nucleotide variant
(missense variant +2 more)
Retinitis pigmentosa
+1 more
GBenign/Likely benign