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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
MYOC
(Q368*)
Single nucleotide variant
(nonsense)
Glaucoma of childhood
GPathogenic
ATM
(N230fs)
Deletion
(frameshift variant)
Hereditary cancer-predisposing syndrome
+6 more
GPathogenic/Likely pathogenic
SLC37A4
(N27K)
Single nucleotide variant
(missense variant +1 more)
Glycogen storage disease, type I
+1 more
GConflicting classifications of pathogenicity
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