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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
APOB
(I2236T)
Single nucleotide variant
(missense variant)
Cardiovascular phenotype
+2 more
GUncertain significance
APOB
(E1965*)
Single nucleotide variant
(nonsense)
Familial hypobetalipoproteinemia 1
GLikely pathogenic
APOB
(P877L)
Single nucleotide variant
(missense variant)
Hypercholesterolemia, autosomal dominant, type B
+4 more
GConflicting classifications of pathogenicity
APOB
(F697V)
Single nucleotide variant
(missense variant)
Familial hypobetalipoproteinemia 1
GUncertain significance
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