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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
FMN2
(P1112del +1 more)
Microsatellite
(inframe_deletion +1 more)
Intellectual disability, autosomal recessive 47
+1 more
GBenign/Likely benign
FMN2
Single nucleotide variant
(synonymous variant)
not specified
+2 more
GBenign/Likely benign