Variant (rsID / SNP)

rs4520

rs4520 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to APOC3. Location: chromosome 11, position 116,701,535. Clinical significance in the table: Benign.

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Reference-table entries

APOC3Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 11:116701535
Cytoband: 11q23.3
HGVS: NM_000040.3(APOC3):c.102T>C (p.Gly34=)
Allele change: Synonymous_G34G

Associated conditions / phenotypes

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.