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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
PCSK9
(P71L)
Single nucleotide variant
(missense variant)
Hypercholesterolemia, autosomal dominant, 3
+4 more
GConflicting classifications of pathogenicity
PCSK9
Single nucleotide variant
(synonymous variant +1 more)
Hypercholesterolemia, familial, 1
+5 more
GConflicting classifications of pathogenicity
PCSK9
(D367H +5 more)
Single nucleotide variant
(missense variant)
Hypercholesterolemia, autosomal dominant, 3
+5 more
GConflicting classifications of pathogenicity
PCSK9
(P479L +6 more)
Single nucleotide variant
(missense variant)
not specified
+1 more
GUncertain significance
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