Variant (rsID / SNP)

rs201201147

rs201201147 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to APOA5, ZPR1. Location: chromosome 11, position 116,660,983. Clinical significance in the table: Benign.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

APOA5Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 11:116660983
Cytoband: 11q23.3
HGVS: NM_001371904.1(APOA5):c.962A>T (p.His321Leu)
Allele change: Missense_H321L

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.