Variant (rsID / SNP)

rs140621530

rs140621530 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to APOC3. Location: chromosome 11, position 116,701,613. Clinical significance in the table: Likely benign.

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Reference-table entries

APOC3Likely benign

Clinical significance (as recorded): Likely benign
Variant type: single nucleotide variant
Chromosome / position: 11:116701613
Cytoband: 11q23.3
HGVS: NM_000040.3(APOC3):c.179+1G>T
Allele change: Silent

Associated conditions / phenotypes

Coronary heart disease|Apolipoprotein c-III deficiency

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.