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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC126860392, RP1
Single nucleotide variant
(synonymous variant +1 more)
not provided
+1 more
GLikely benign
LOC126860392, RP1
(R1652C)
Single nucleotide variant
(missense variant +1 more)
RP1-related condition
+1 more
GLikely benign
LOC126860392, RP1
Single nucleotide variant
(synonymous variant +1 more)
not provided
+1 more
GLikely benign
LOC126860392, RP1
(G1875A)
Single nucleotide variant
(missense variant)
not provided
+3 more
GLikely benign
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