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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SLITRK6
(Q414*)
Single nucleotide variant
(nonsense)
SLITRK6-related condition
+2 more
GPathogenic/Likely pathogenic
SLITRK6
(S297*)
Single nucleotide variant
(nonsense)
High myopia-sensorineural deafness syndrome
GLikely pathogenic
SLITRK6
(R181*)
Single nucleotide variant
(nonsense)
High myopia-sensorineural deafness syndrome
GPathogenic
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