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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ACADM, ACOT11
+570 more
Copy number gain
See cases
GPathogenic
ACOT11, BSND
+205 more
Copy number loss
See cases
GPathogenic
ACOT11, FAM151A
(A416V)
Single nucleotide variant
(3 prime UTR variant +2 more)
not provided
GBenign
ACOT11, FAM151A
Single nucleotide variant
(intron variant)
not provided
GBenign
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