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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
PCDH15
Single nucleotide variant
(intron variant)
Retinal dystrophy
+1 more
GUncertain significance
PCDH15
Single nucleotide variant
(splice donor variant)
Retinal dystrophy
GLikely pathogenic
PCDH15
(Y579* +5 more)
Single nucleotide variant
(nonsense)
Usher syndrome type 1F
+5 more
GPathogenic/Likely pathogenic
PCDH15
(Q92* +2 more)
Single nucleotide variant
(nonsense)
Usher syndrome type 1F
+3 more
GPathogenic/Likely pathogenic
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