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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
DMXL2
(E977del +1 more)
Deletion
(inframe_deletion +2 more)
not provided
GUncertain significance
DMXL2
(R749Q +1 more)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance