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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
DENND5A, DNHD1
+723 more
Copy number gain
See cases
GPathogenic
LOC130005165, STIM1
(V5I)
Single nucleotide variant
(missense variant +4 more)
Stormorken syndrome
+3 more
GUncertain significance