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Items: 6

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
RP1
(R872H)
Single nucleotide variant
(missense variant)
not specified
+4 more
GBenign
RP1
(N985Y)
Single nucleotide variant
(missense variant)
Retinal dystrophy
+4 more
GBenign/Likely benign
LOC126860392, RP1
(A1670T)
Single nucleotide variant
(missense variant)
Retinal dystrophy
+4 more
GBenign
LOC126860392, RP1
(S1691P)
Single nucleotide variant
(missense variant)
Retinal dystrophy
+4 more
GBenign
LOC126860392, RP1
Single nucleotide variant
(synonymous variant)
Retinal dystrophy
+4 more
GBenign
RP1
(C2033Y)
Single nucleotide variant
(missense variant)
Retinal dystrophy
+4 more
GBenign/Likely benign
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