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Variant (rsID / SNP)

rs76353203

APOC3

rs76353203 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to APOC3. Location: chromosome 11, position 116,701,353. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

APOC3Conflicting interpretations
Clinical significance (as recorded)
Conflicting interpretations of pathogenicity
Variant type
single nucleotide variant
Chromosome / position
11:116701353
Cytoband
11q23.3
HGVS
NM_000040.3(APOC3):c.55C>T (p.Arg19Ter)
Allele change
Nonsense_R19X

Associated conditions / phenotypes

Apolipoprotein c-III deficiency|Coronary heart disease

Public references

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