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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CKMT1A, CTDSPL2
+42 more
Copy number loss
See cases
GUncertain significance
B2M, CTDSPL2
+21 more
Duplication
See cases
GUncertain significance
EIF3J, LOC130056969
(D23N)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
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