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Variant (rsID / SNP)

rs147210663

APOC3

rs147210663 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to APOC3. Location: chromosome 11, position 116,701,560. 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
11:116701560
Cytoband
11q23.3
HGVS
NM_000040.3(APOC3):c.127G>A (p.Ala43Thr)
Allele change
Missense_A43T

Associated conditions / phenotypes

Coronary heart disease|Apolipoprotein c-III deficiency

Public references

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