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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ACAT2, AFDN
+549 more
Copy number loss
See cases
GPathogenic
SLC22A3
Single nucleotide variant
(5 prime UTR variant)
not provided
GBenign
SLC22A3
Single nucleotide variant
(intron variant)
not provided
GBenign
SLC22A3
Single nucleotide variant
(synonymous variant)
not provided
GBenign
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