Variant (rsID / SNP)

rs769455

rs769455 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to APOE. Location: chromosome 19, position 45,412,040. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

APOEConflicting interpretations

Clinical significance (as recorded): Conflicting interpretations of pathogenicity
Variant type: single nucleotide variant
Chromosome / position: 19:45412040
Cytoband: 19q13.32
HGVS: NM_000041.4(APOE):c.487C>T (p.Arg163Cys)
Allele change: Missense_R163C

Associated conditions / phenotypes

Familial type 3 hyperlipoproteinemia

Public references

dbSNP
ClinVar
Ensembl
gnomAD

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