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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
MAGEL2
(W965*)
Single nucleotide variant
(nonsense)
Prader-Willi syndrome
GPathogenic
MAGEL2
(V701fs)
Duplication
(frameshift variant)
Prader-Willi syndrome
GPathogenic