Variant (rsID / SNP)

rs15285

rs15285 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LPL. Location: chromosome 8, position 19,824,667. Clinical significance in the table: Benign.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

LPLBenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 8:19824667
Cytoband: 8p21.3
HGVS: NM_000237.3(LPL):c.*1846C>T
Allele change: Missense_H1092Y

Associated conditions / phenotypes

Hyperlipoproteinemia, type I

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.