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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SLC30A9
(S14fs)
Deletion
(frameshift variant)
not provided
+1 more
GConflicting classifications of pathogenicity
SLC30A9
Single nucleotide variant
(splice donor variant)
Psychomotor regression-oculomotor apraxia-movement disorder-nephropathy syndrome
GLikely pathogenic