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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CHKB-CPT1B, CPT1B
Single nucleotide variant
(intron variant)
not specified
+1 more
GBenign/Likely benign
CHKB-CPT1B, CPT1B
Single nucleotide variant
(intron variant)
not specified
GBenign
CHKB, CHKB-CPT1B
(Q328R)
Single nucleotide variant
(missense variant +1 more)
not specified
+2 more
GConflicting classifications of pathogenicity
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