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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
EFTUD2
(Y687* +2 more)
Single nucleotide variant
(nonsense)
Mandibulofacial dysostosis-microcephaly syndrome
GLikely pathogenic
EFTUD2
(A641fs +2 more)
Duplication
(frameshift variant)
Mandibulofacial dysostosis-microcephaly syndrome
GLikely pathogenic
EFTUD2
Single nucleotide variant
(splice acceptor variant)
Mandibulofacial dysostosis-microcephaly syndrome
GLikely pathogenic
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