Variant (rsID / SNP)

rs2266788

rs2266788 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to APOA5, ZPR1. Location: chromosome 11, position 116,660,686. Clinical significance in the table: Benign.

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Reference-table entries

APOA5Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 11:116660686
Cytoband: 11q23.3
HGVS: NM_001371904.1(APOA5):c.*158C>T
Allele change: Silent

Associated conditions / phenotypes

Hypertriglyceridemia, familial

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.