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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
APOB, APOB3'MAR
(E4558K)
Single nucleotide variant
(missense variant)
Familial hypercholesterolemia
+2 more
GUncertain significance
APOB, APOB3'MAR
(T4536M)
Single nucleotide variant
(missense variant)
Hypercholesterolemia, autosomal dominant, type B
+2 more
GConflicting classifications of pathogenicity
APOB, APOB3'MAR
(Y4534C)
Single nucleotide variant
(missense variant)
Hypercholesterolemia, familial, 1
+3 more
GUncertain significance
APOB, APOB3'MAR
(H4529R)
Single nucleotide variant
(missense variant)
Familial hypobetalipoproteinemia 1
+3 more
GConflicting classifications of pathogenicity
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