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Links from OMIM

Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
COMT
(V158M +1 more)
Single nucleotide variant
(missense variant)
not specified
+2 more
GBenign
MAOA
Microsatellite
Autism, severe
+1 more
GPathogenic; risk factor