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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CPAMD8
(Q639R)
Single nucleotide variant
(missense variant +1 more)
Anterior segment dysgenesis 8
GUncertain significance
CPAMD8
(R58M)
Single nucleotide variant
(missense variant +1 more)
not provided
+2 more
GConflicting classifications of pathogenicity
CPAMD8
Single nucleotide variant
(5 prime UTR variant +1 more)
Anterior segment dysgenesis 8
GLikely pathogenic
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