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Items: 9

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
APOB
(T4484M)
Single nucleotide variant
(missense variant)
Cardiovascular phenotype
+5 more
GConflicting classifications of pathogenicity
APOB
(I4314V)
Single nucleotide variant
(missense variant)
Cardiovascular phenotype
+5 more
GConflicting classifications of pathogenicity
APOB
(N3213K)
Single nucleotide variant
(missense variant)
not specified
+4 more
GConflicting classifications of pathogenicity
APOB
Single nucleotide variant
(synonymous variant)
Cardiovascular phenotype
+3 more
GConflicting classifications of pathogenicity
APOB
(E1734del)
Microsatellite
(inframe_deletion)
not provided
GUncertain significance
APOB
(R1128H)
Single nucleotide variant
(missense variant)
APOB-related condition
+7 more
GConflicting classifications of pathogenicity
APOB
(K768E)
Single nucleotide variant
(missense variant)
Cardiovascular phenotype
+1 more
GUncertain significance
APOB
(A345T)
Single nucleotide variant
(missense variant)
Cardiovascular phenotype
+3 more
GConflicting classifications of pathogenicity
APOB
(A251T)
Single nucleotide variant
(missense variant)
Cardiovascular phenotype
+6 more
GBenign/Likely benign
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