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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC130001226, LOC130001227
+1407 more
Copy number gain
See cases
GPathogenic
RIMS2
(R1098L +22 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance