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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
GNAT2
(H282fs)
Insertion
(frameshift variant)
Achromatopsia 4
GPathogenic
GNAT2
Single nucleotide variant
(intron variant)
Achromatopsia 4
GConflicting classifications of pathogenicity
GNAT2
(A96fs)
Indel
(frameshift variant)
Achromatopsia 4
GPathogenic
GNAT2
(Q79*)
Single nucleotide variant
(nonsense)
not provided
GPathogenic
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