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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LPL
(P234L)
Single nucleotide variant
(missense variant)
Hyperlipoproteinemia, type I
+3 more
GPathogenic/Likely pathogenic
LPL
(H268Q)
Single nucleotide variant
(missense variant)
Hyperlipidemia, familial combined, LPL related
GUncertain significance
LPL
(C305S)
Single nucleotide variant
(missense variant)
Hyperlipidemia, familial combined, LPL related
+1 more
GConflicting classifications of pathogenicity
LPL
(N318S)
Single nucleotide variant
(missense variant)
Cardiovascular phenotype
+4 more
GConflicting classifications of pathogenicity
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