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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SLC24A1
(Q161*)
Single nucleotide variant
(nonsense)
Retinal dystrophy
+1 more
GPathogenic/Likely pathogenic
SLC24A1
(A227fs)
Deletion
(frameshift variant)
Retinal dystrophy
GLikely pathogenic
SLC24A1
(M252fs)
Deletion
(frameshift variant)
not provided
+3 more
GPathogenic
SLC24A1
(S378fs)
Deletion
(frameshift variant)
not provided
+1 more
GPathogenic/Likely pathogenic
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