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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
OS9
(L15V)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
OS9
(S103T)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
OS9
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
OS9
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
AGAP2, ARHGAP9
+45 more
Copy number loss
not provided
GLikely pathogenic
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