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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
C14orf39
(F427L)
Single nucleotide variant
(missense variant)
C14orf39-related condition
GLikely benign
C14orf39, SIX6
(E129K)
Single nucleotide variant
(missense variant)
SIX6-related disorder
+4 more
GConflicting classifications of pathogenicity
C14orf39, SIX6
(H141N)
Single nucleotide variant
(missense variant)
Colobomatous optic disc-macular atrophy-chorioretinopathy syndrome
+3 more
GBenign
C14orf39, SIX6
(I246N)
Single nucleotide variant
(missense variant)
not provided
+1 more
GLikely benign
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