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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
RAB41
Single nucleotide variant
(intron variant)
not provided
GLikely benign
RAB41
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
RAB41
Single nucleotide variant
(3 prime UTR variant)
not provided
GLikely benign
TMEM31, TMEM35A
+488 more
Copy number gain
not provided
GPathogenic
AWAT2, BCLAF3
+568 more
Copy number gain
not provided
GUncertain significance
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