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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
OTUD7A
(G876R +1 more)
Single nucleotide variant
(missense variant)
See cases
GUncertain significance
CHRNA7, LOC125078053
+3 more
Duplication
15q11q13 microduplication syndrome
GUncertain significance