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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
KLHL7
(T143fs +1 more)
Duplication
(frameshift variant +1 more)
KLHL7-related disorder
GLikely pathogenic
KLHL7
(L146del +1 more)
Microsatellite
(inframe_deletion +1 more)
KLHL7-related disorder
GLikely pathogenic