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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC130068854, MECP2
Microsatellite
(5 prime UTR variant +1 more)
Rett syndrome
GBenign
LOC130068854, MECP2
Microsatellite
(inframe_deletion +1 more)
Rett syndrome
GBenign