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Variant (rsID / SNP)

rs1799812

APOB

rs1799812 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to APOB. Location: chromosome 2, position 21,229,609. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

APOBConflicting interpretations
Clinical significance (as recorded)
Conflicting interpretations of pathogenicity
Variant type
single nucleotide variant
Chromosome / position
2:21229609
Cytoband
2p24.1
HGVS
NM_000384.3(APOB):c.10131G>A (p.Leu3377=)
Allele change
Synonymous_L3377L

Associated conditions / phenotypes

Hypercholesterolemia, familial, 1|Familial hypercholesterolemia|Hypercholesterolemia, autosomal dominant, type B|Familial hypobetalipoproteinemia 1|Hypercholesterolemia, autosomal dominant, type B|Familial hypobetalipoproteinemia 1

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.