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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CETP
(L290P)
Single nucleotide variant
(missense variant +1 more)
not provided
+1 more
GUncertain significance
CETP
Single nucleotide variant
(intron variant)
not provided
GUncertain significance
CETP
(K287E +1 more)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
CETP
(D459G +1 more)
Single nucleotide variant
(missense variant)
Hyperalphalipoproteinemia 1
+1 more
GConflicting classifications of pathogenicity
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