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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
MAGI2, MAGI2-AS3
Single nucleotide variant
(non-coding transcript variant +1 more)
MAGI2-related condition
+3 more
GBenign/Likely benign
MAGI2-AS3, MAGI2
Single nucleotide variant
(non-coding transcript variant +1 more)
MAGI2-related condition
+2 more
GConflicting classifications of pathogenicity
MAGI2, MAGI2-AS3
(S4I)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
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