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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
MBOAT7
(E376K +1 more)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
MBOAT7
(P36L +1 more)
Single nucleotide variant
(missense variant +1 more)
Intellectual disability, autosomal recessive 57
GLikely pathogenic