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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
APOB
(E3788K)
Single nucleotide variant
(missense variant)
Familial hypobetalipoproteinemia 1
+2 more
GConflicting classifications of pathogenicity
APOB
(S2429T)
Single nucleotide variant
(missense variant)
Cardiovascular phenotype
+6 more
GConflicting classifications of pathogenicity
APOB
(D550H)
Single nucleotide variant
(missense variant)
not provided
+2 more
GConflicting classifications of pathogenicity
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