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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
APOB
(R3558C)
Single nucleotide variant
(missense variant)
Cardiovascular phenotype
+5 more
GUncertain significance
APOB
(R3527Q)
Single nucleotide variant
(missense variant)
Homozygous familial hypercholesterolemia
+10 more
GPathogenic/Likely pathogenic
APOB
(R3527W)
Single nucleotide variant
(missense variant)
APOB-related condition
+8 more
GPathogenic/Likely pathogenic
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