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Variant (rsID / SNP)

rs121918390

APOB

rs121918390 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to APOB. Location: chromosome 2, position 21,232,176. 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
2:21232176
Cytoband
2p24.1
HGVS
NM_000384.3(APOB):c.7564C>T (p.Arg2522Ter)
Allele change
Nonsense_R2522X

Associated conditions / phenotypes

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

Public references

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