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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
RAI1
(Q291del)
Microsatellite
(inframe_deletion)
RAI1-related condition
+4 more
GBenign
RAI1
(E1261del)
Microsatellite
(inframe_deletion)
Inborn genetic diseases
+4 more
GBenign/Likely benign