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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
MBOAT7, TSEN34
Single nucleotide variant
(5 prime UTR variant +1 more)
Intellectual disability, autosomal recessive 57
+1 more
GLikely benign
TSEN34
(S131L)
Single nucleotide variant
(missense variant)
not specified
+3 more
GUncertain significance