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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
AATK, ACTG1
+385 more
Copy number gain
See cases
GPathogenic
ACTG1, LOC130061941
Single nucleotide variant
(intron variant)
not provided
GBenign
ACTG1, LOC130061941
Single nucleotide variant
(intron variant)
not specified
+1 more
GLikely benign
ACTG1, LOC130061941
Single nucleotide variant
(5 prime UTR variant +1 more)
not provided
GLikely benign
ACTG1, LOC130061941
Single nucleotide variant
(5 prime UTR variant +1 more)
not provided
GBenign
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