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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
AMT
(R320C +2 more)
Single nucleotide variant
(missense variant +1 more)
Non-ketotic hyperglycinemia
+1 more
GPathogenic/Likely pathogenic
AMT
(L210P +2 more)
Single nucleotide variant
(missense variant +1 more)
Non-ketotic hyperglycinemia
GConflicting classifications of pathogenicity
AMT
Deletion
(splice donor variant)
Inborn genetic diseases
+1 more
GLikely pathogenic
AMT, NICN1
(S6fs)
Deletion
(frameshift variant +2 more)
not provided
+1 more
GPathogenic/Likely pathogenic
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