Variant (rsID / SNP)
rs326
rs326 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LPL. Location: chromosome 8, position 19,819,439. Clinical significance in the table: Benign.
Reference-table entries
LPLBenign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 8:19819439
- Cytoband
- 8p21.3
- HGVS
- NM_000237.3(LPL):c.1323-187A>G
- Allele change
- Silent
Associated conditions / phenotypes
High density lipoprotein cholesterol level quantitative trait locus 11
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.