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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SVBP
(Q28*)
Single nucleotide variant
(nonsense)
Neurodevelopmental disorder with ataxia, hypotonia, and microcephaly
+4 more
GPathogenic/Likely pathogenic
ATP6V0A1
(R741Q +22 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+12 more
GConflicting classifications of pathogenicity