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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
NSFL1C
(L191F +2 more)
Single nucleotide variant
(missense variant +1 more)
not provided
GLikely benign
SLC24A3, SLC4A11
+164 more
Copy number gain
not provided
GPathogenic
TRIB3, TRMT6
+114 more
Copy number gain
not provided
GPathogenic
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