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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
BPNT2, CERNA3
+105 more
Copy number loss
See cases
GPathogenic
CYP7A1, LOC126860400
Single nucleotide variant
(intron variant)
not provided
GBenign
CYP7A1, LOC126860400
Single nucleotide variant
(intron variant)
not provided
GBenign
CYP7A1, LOC126860400
Single nucleotide variant
(intron variant)
not provided
GLikely benign
CYP7A1, LOC126860400
Deletion
(intron variant)
not provided
GBenign/Likely benign
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