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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC100505774, LOC129388837
+14 more
Copy number gain
See cases
GUncertain significance
LOC129933407, PPP1CB
Single nucleotide variant
not provided
GBenign
LOC129933407, PPP1CB
Single nucleotide variant
(5 prime UTR variant)
not provided
GLikely benign
PPP1CB, LOC129933407
Single nucleotide variant
(5 prime UTR variant)
not provided
GBenign
PPP1CB, LOC129933407
Single nucleotide variant
(5 prime UTR variant)
not provided
GBenign
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