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Links from MedGen

Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SVBP
(K13fs)
Deletion
(frameshift variant)
Microcephaly
+2 more
GPathogenic
SVBP
(Q28*)
Single nucleotide variant
(nonsense)
Neurodevelopmental disorder with ataxia, hypotonia, and microcephaly
+4 more
GPathogenic/Likely pathogenic