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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
MBOAT7
(L306fs +1 more)
Deletion
(frameshift variant)
Intellectual disability, autosomal recessive 57
GLikely pathogenic
MBOAT7
(Y281* +1 more)
Single nucleotide variant
(nonsense)
Intellectual disability, autosomal recessive 57
GPathogenic