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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC129996415, LOC129996416
+435 more
Copy number loss
See cases
GPathogenic
KCNK16, KCNK17
(S21G)
Single nucleotide variant
(missense variant)
not provided
GBenign