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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
MBOAT7
(Y281* +1 more)
Single nucleotide variant
(nonsense)
Intellectual disability, autosomal recessive 57
GPathogenic
MBOAT7
(R198fs +1 more)
Duplication
(frameshift variant)
Intellectual disability, autosomal recessive 57
GLikely pathogenic
MBOAT7
Deletion
(inframe_deletion)
Intellectual disability, autosomal recessive 57
+2 more
GPathogenic
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