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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SLITRK6
(S754L)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
SLITRK6
(A371V)
Single nucleotide variant
(missense variant)
High myopia-sensorineural deafness syndrome
GUncertain significance
SLITRK6
(S297*)
Single nucleotide variant
(nonsense)
High myopia-sensorineural deafness syndrome
GLikely pathogenic
SLITRK6
Single nucleotide variant
(synonymous variant)
not specified
+2 more
GBenign/Likely benign
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