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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC126860392, RP1
(R1668G)
Single nucleotide variant
(missense variant +1 more)
not provided
+1 more
GUncertain significance
RP1, LOC126860392
(L1901F)
Single nucleotide variant
(missense variant)
not provided
+2 more
GBenign/Likely benign