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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC130055392, LOC130055393
+780 more
Copy number gain
See cases
GPathogenic
LOC130055324, SLC7A7
Single nucleotide variant
(5 prime UTR variant)
not specified
+2 more
GLikely benign