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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
HNMT
(E109K)
Single nucleotide variant
(missense variant)
Intellectual disability, autosomal recessive 51
+1 more
GConflicting classifications of pathogenicity
HNMT
Single nucleotide variant
(synonymous variant)
Intellectual disability, autosomal recessive 51
GUncertain significance